Is this your brand? Sign in to claim ownership.

KING SYSTEMS CORPORATION.

Last updated September 17, 2026

Information

Country: US
Address: 15011 HERRIMAN BLVD., Noblesville, IN, 46060
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 1824226
DUNS Number: —

Catalogue (1113)

Page 3 of 23

Device	Model / Reference	Registries	Class	Status
Universal F® Flex2®	JAF3116-6121Z	FDA UDI	Class I	Active
Custom Accessory	D023	FDA UDI	Class I	Active
Universal F2®anesthesia Breathing Circuit	D466-6121Z	FDA UDI	Class I	Active
Pediatric Ultra Flex®anesthesia Breathing Circuit	2907V-61	FDA UDI	Class I	Unknown
Universal F® Flexbreathing Circuit	GHUF3116-6121Z	FDA UDI	Class I	Active
Universal F2®breathing Circuit & Pack Kit	F90575	FDA UDI	Class I	Unknown
Universal Flex2®breathing Circuit	DF375-176Z	FDA UDI	Class I	Unknown
Universal Flex2®breathing Circuit	DF070-6121	FDA UDI	Class I	Active
Universal Flex2®breathing Circuit & Pack Kit	F90732	FDA UDI	Class I	Unknown
Universal Flex2®breathing Circuit	DF4115-6121Z	FDA UDI	Class I	Active
Universal Flex2®breathing Circuit	SJDF3116-6121Z	FDA UDI	Class I	Active
King LTS-D	KLTSD425	FDA UDI	Class I	Active
Pediatric Ultra Flex®anesthesia Circuit & Pack Kit	94490	FDA UDI	Class I	Active
Jackson Rees	3773-WSZ	FDA UDI	Class I	Active
Universal F2®anesthesia Breathing Circuit	D495-6121Z	FDA UDI	Class I	Active
Universal F2®anesthesia Breathing Circuit	D060-8021	FDA UDI	Class I	Active
Universal F2®anesthesia Breathing Circuit	D495-61Z	FDA UDI	Class I	Active
Corrugated Tubing	101100	FDA UDI	Class I	Active
Universal Flex2®breathing Circuit	DFP170-17621	FDA UDI	Class I	Active
Universal Flex2®	F99008	FDA UDI	Class I	Active
Universal Flex2®breathing Circuit	DFP170-61	FDA UDI	Class I	Active
Universal F2®anesthesia Breathing Circuit	D395-6121Z	FDA UDI	Class I	Active
Adult Anesthesia	8603B-61Z	FDA UDI	Class I	Active
Breathing Bag	5098	FDA UDI	Class I	Active
Universal Flex2®breathing Circuit	KNCF476-6121Z	FDA UDI	Class I	Active
Universal F2®anesthesia Breathing Circuit	D365-8033Z	FDA UDI	Class I	Unknown
Ped F2® Pediatricbreathing Circuit	DSNPCP160-618	FDA UDI	Class I	Unknown
Universal F®	U0120-61	FDA UDI	Class I	Active
Universal Flex2®breathing Circuit	DF470-17621Z	FDA UDI	Class I	Active
Disposable Xenon Circuitfor Nuclear Medicine	21126	FDA UDI	Class II	Active
Disposable Xenon Circuitfor Nuclear Medicine	24126	FDA UDI	Class II	Active
Universal Flex2®breathing Circuit	DF3110-6121Z	FDA UDI	Class I	Active
Ped F2® Pediatric	PCP160-61	FDA UDI	Class I	Active
Adult Ultra Flex®	51213F-14621Z	FDA UDI	Class I	Active
Ped F2® Pediatricanesthesia Circuit & Pack Kit	F90579	FDA UDI	Class I	Active
Universal Flex2®breathing Circuit	DF370-6133Z	FDA UDI	Class I	Unknown
Adult Ultra Flex®	81813F-136Z	FDA UDI	Class I	Active
Universal Flex2®breathing Circuit	KNCF370-6121Z	FDA UDI	Class I	Active
Universal Flex2®breathing Circuit	DFP270-61	FDA UDI	Class I	Active
Jackson Rees	3771Z	FDA UDI	Class I	Active
Adult Ultra Flex®anesthesia Breathing Circuit	QR6753F-8421AEZ	FDA UDI	Class I	Active
Universal F2®	XF60	FDA UDI	Class I	Active
Adult Anesthesiabreathing Circuit	V5403F-61Z	FDA UDI	Class I	Unknown
Universal F2®anesthesia Breathing Circuit	D490-60Z	FDA UDI	Class I	Unknown
Pediatric Ultra Flex®anesthesia Breathing Circuit	2706P-164	FDA UDI	Class I	Active
Universal Flex2®breathing Circuit & Pack Kit	F94939	FDA UDI	Class I	Active
Ped F2® Pediatricanesthesia Breathing Circuit	PDP240-6121	FDA UDI	Class I	Active
Adult Ultra Flex®	81214F-19121Z	FDA UDI	Class I	Active
Ped F2® Pediatricanesthesia Circuit & Pack Kit	F90542Z	FDA UDI	Class I	Unknown
Mapleson D Circuit	4842P-61	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (100)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Feb 17, 2015	Z-1361-2015	—	terminated	Product is mislabeled as Double Swivel Connector with Suction Port and is actually Double Swivel Connector without Suction port. If the incorrect component is not identified prior to clinical use, the incorrect connector would be replaced during the case without risk to the patient and could result in a short delay of the procedure.
Sep 3, 2013	Z-2255-2013	—	terminated	Report that size 5 KLTD airways were packaged in pouches indicating a size of 2.5 and shipped to your facility. The correct size of the KLTD airway is clearly marked on the actual airway product and the physical size difference between 2.5 and 5 is distinct and obvious.
Nov 2, 2012	Z-0426-2013	—	terminated	The firm received two complaints from a user facility in New Jersey regarding color-coded EtO sterilization indicators on the primary device packaging that did not undergo the expected color change. The complainant reported devices that had pink color indicators when the product packaging specified that the color should change from pink to yellow (or brown) if the product had subjected to an EtO
Nov 2, 2012	Z-0420-2013	—	terminated	The firm received two complaints from a user facility in New Jersey regarding color-coded EtO sterilization indicators on the primary device packaging that did not undergo the expected color change. The complainant reported devices that had pink color indicators when the product packaging specified that the color should change from pink to yellow (or brown) if the product had subjected to an EtO
Nov 2, 2012	Z-0421-2013	—	terminated	The firm received two complaints from a user facility in New Jersey regarding color-coded EtO sterilization indicators on the primary device packaging that did not undergo the expected color change. The complainant reported devices that had pink color indicators when the product packaging specified that the color should change from pink to yellow (or brown) if the product had subjected to an EtO
Nov 2, 2012	Z-0418-2013	—	terminated	The firm received two complaints from a user facility in New Jersey regarding color-coded EtO sterilization indicators on the primary device packaging that did not undergo the expected color change. The complainant reported devices that had pink color indicators when the product packaging specified that the color should change from pink to yellow (or brown) if the product had subjected to an EtO
Nov 2, 2012	Z-0419-2013	—	terminated	The firm received two complaints from a user facility in New Jersey regarding color-coded EtO sterilization indicators on the primary device packaging that did not undergo the expected color change. The complainant reported devices that had pink color indicators when the product packaging specified that the color should change from pink to yellow (or brown) if the product had subjected to an EtO
Nov 2, 2012	Z-0425-2013	—	terminated	The firm received two complaints from a user facility in New Jersey regarding color-coded EtO sterilization indicators on the primary device packaging that did not undergo the expected color change. The complainant reported devices that had pink color indicators when the product packaging specified that the color should change from pink to yellow (or brown) if the product had subjected to an EtO
Nov 2, 2012	Z-0427-2013	—	terminated	The firm received two complaints from a user facility in New Jersey regarding color-coded EtO sterilization indicators on the primary device packaging that did not undergo the expected color change. The complainant reported devices that had pink color indicators when the product packaging specified that the color should change from pink to yellow (or brown) if the product had subjected to an EtO
Nov 2, 2012	Z-0423-2013	—	terminated	The firm received two complaints from a user facility in New Jersey regarding color-coded EtO sterilization indicators on the primary device packaging that did not undergo the expected color change. The complainant reported devices that had pink color indicators when the product packaging specified that the color should change from pink to yellow (or brown) if the product had subjected to an EtO
Nov 2, 2012	Z-0424-2013	—	terminated	The firm received two complaints from a user facility in New Jersey regarding color-coded EtO sterilization indicators on the primary device packaging that did not undergo the expected color change. The complainant reported devices that had pink color indicators when the product packaging specified that the color should change from pink to yellow (or brown) if the product had subjected to an EtO
Nov 2, 2012	Z-0422-2013	—	terminated	The firm received two complaints from a user facility in New Jersey regarding color-coded EtO sterilization indicators on the primary device packaging that did not undergo the expected color change. The complainant reported devices that had pink color indicators when the product packaging specified that the color should change from pink to yellow (or brown) if the product had subjected to an EtO
Aug 23, 2012	Z-2272-2013	—	terminated	King Systems received a customer complaint indicating that the customer had ordered a breathing circuit with a Latex breathing bag. The product they received contained a Latex breathing bag, but was labeled as non-latex.
Jan 24, 2011	Z-1889-2011	—	terminated	The firm is conducting a subrecall of facetent masks because the masks could have a sticky substance on the inside or outside of the mask that may manifest itself 6-8 months after the manufacture date of the product. The sticky substance could result in inconvenience or in some remote cases cause patient harm.
Jan 24, 2011	Z-1879-2011	—	terminated	The firms contract manufacturer reported that the products were below the specification for hardness. This could contribute to a higher incidence of problems during the insertion and final positioning of the airway in the patient. In rare instances the softness of the tube could cause the tube to fold over.
Jan 24, 2011	Z-1888-2011	—	terminated	The firm is conducting a subrecall of facetent masks because the masks could have a sticky substance on the inside or outside of the mask that may manifest itself 6-8 months after the manufacture date of the product. The sticky substance could result in inconvenience or in some remote cases cause patient harm.
Jan 24, 2011	Z-1890-2011	—	terminated	The firm is conducting a subrecall of facetent masks because the masks could have a sticky substance on the inside or outside of the mask that may manifest itself 6-8 months after the manufacture date of the product. The sticky substance could result in inconvenience or in some remote cases cause patient harm.
Jan 24, 2011	Z-1887-2011	—	terminated	The firm is conducting a subrecall of facetent masks because the masks could have a sticky substance on the inside or outside of the mask that may manifest itself 6-8 months after the manufacture date of the product. The sticky substance could result in inconvenience or in some remote cases cause patient harm.
Jan 24, 2011	Z-1892-2011	—	terminated	The firm is conducting a subrecall of facetent masks because the masks could have a sticky substance on the inside or outside of the mask that may manifest itself 6-8 months after the manufacture date of the product. The sticky substance could result in inconvenience or in some remote cases cause patient harm.
Jan 24, 2011	Z-1878-2011	—	terminated	The firms contract manufacturer reported that the products were below the specification for hardness. This could contribute to a higher incidence of problems during the insertion and final positioning of the airway in the patient. In rare instances the softness of the tube could cause the tube to fold over.
Jan 24, 2011	Z-1891-2011	—	terminated	The firm is conducting a subrecall of facetent masks because the masks could have a sticky substance on the inside or outside of the mask that may manifest itself 6-8 months after the manufacture date of the product. The sticky substance could result in inconvenience or in some remote cases cause patient harm.
Jan 14, 2011	Z-1718-2011	—	terminated	King Systems has been notified by Triad Group, our supplier of sterile lubricating jelly, that a recall has been initiated for this product because the product may be "inadequately sterilized" and use of this product may result in "patient infection". Because this particular sterile lubricating jelly is packaged in the KING LT-D Kit and KING LTS-D Kit, King Systems is sending a Notice of the Reca
Jan 14, 2011	Z-1706-2011	—	terminated	King Systems has been notified by Triad Group, our supplier of sterile lubricating jelly, that a recall has been initiated for this product because the product may be "inadequately sterilized" and use of this product may result in "patient infection". Because this particular sterile lubricating jelly is packaged in the KING LT-D Kit and KING LTS-D Kit, King Systems is sending a Notice of the Reca
Jan 14, 2011	Z-1714-2011	—	terminated	King Systems has been notified by Triad Group, our supplier of sterile lubricating jelly, that a recall has been initiated for this product because the product may be "inadequately sterilized" and use of this product may result in "patient infection". Because this particular sterile lubricating jelly is packaged in the KING LT-D Kit and KING LTS-D Kit, King Systems is sending a Notice of the Reca
Jan 14, 2011	Z-1720-2011	—	terminated	King Systems has been notified by Triad Group, our supplier of sterile lubricating jelly, that a recall has been initiated for this product because the product may be "inadequately sterilized" and use of this product may result in "patient infection". Because this particular sterile lubricating jelly is packaged in the KING LT-D Kit and KING LTS-D Kit, King Systems is sending a Notice of the Reca
Jan 14, 2011	Z-1721-2011	—	terminated	King Systems has been notified by Triad Group, our supplier of sterile lubricating jelly, that a recall has been initiated for this product because the product may be "inadequately sterilized" and use of this product may result in "patient infection". Because this particular sterile lubricating jelly is packaged in the KING LT-D Kit and KING LTS-D Kit, King Systems is sending a Notice of the Reca
Jan 14, 2011	Z-1707-2011	—	terminated	King Systems has been notified by Triad Group, our supplier of sterile lubricating jelly, that a recall has been initiated for this product because the product may be "inadequately sterilized" and use of this product may result in "patient infection". Because this particular sterile lubricating jelly is packaged in the KING LT-D Kit and KING LTS-D Kit, King Systems is sending a Notice of the Reca
Jan 14, 2011	Z-1710-2011	—	terminated	King Systems has been notified by Triad Group, our supplier of sterile lubricating jelly, that a recall has been initiated for this product because the product may be "inadequately sterilized" and use of this product may result in "patient infection". Because this particular sterile lubricating jelly is packaged in the KING LT-D Kit and KING LTS-D Kit, King Systems is sending a Notice of the Reca
Jan 14, 2011	Z-1717-2011	—	terminated	King Systems has been notified by Triad Group, our supplier of sterile lubricating jelly, that a recall has been initiated for this product because the product may be "inadequately sterilized" and use of this product may result in "patient infection". Because this particular sterile lubricating jelly is packaged in the KING LT-D Kit and KING LTS-D Kit, King Systems is sending a Notice of the Reca
Jan 14, 2011	Z-1713-2011	—	terminated	King Systems has been notified by Triad Group, our supplier of sterile lubricating jelly, that a recall has been initiated for this product because the product may be "inadequately sterilized" and use of this product may result in "patient infection". Because this particular sterile lubricating jelly is packaged in the KING LT-D Kit and KING LTS-D Kit, King Systems is sending a Notice of the Reca
Jan 14, 2011	Z-1712-2011	—	terminated	King Systems has been notified by Triad Group, our supplier of sterile lubricating jelly, that a recall has been initiated for this product because the product may be "inadequately sterilized" and use of this product may result in "patient infection". Because this particular sterile lubricating jelly is packaged in the KING LT-D Kit and KING LTS-D Kit, King Systems is sending a Notice of the Reca
Jan 14, 2011	Z-1705-2011	—	terminated	King Systems has been notified by Triad Group, our supplier of sterile lubricating jelly, that a recall has been initiated for this product because the product may be "inadequately sterilized" and use of this product may result in "patient infection". Because this particular sterile lubricating jelly is packaged in the KING LT-D Kit and KING LTS-D Kit, King Systems is sending a Notice of the Reca
Jan 14, 2011	Z-1708-2011	—	terminated	King Systems has been notified by Triad Group, our supplier of sterile lubricating jelly, that a recall has been initiated for this product because the product may be "inadequately sterilized" and use of this product may result in "patient infection". Because this particular sterile lubricating jelly is packaged in the KING LT-D Kit and KING LTS-D Kit, King Systems is sending a Notice of the Reca
Jan 14, 2011	Z-1715-2011	—	terminated	King Systems has been notified by Triad Group, our supplier of sterile lubricating jelly, that a recall has been initiated for this product because the product may be "inadequately sterilized" and use of this product may result in "patient infection". Because this particular sterile lubricating jelly is packaged in the KING LT-D Kit and KING LTS-D Kit, King Systems is sending a Notice of the Reca
Jan 14, 2011	Z-1709-2011	—	terminated	King Systems has been notified by Triad Group, our supplier of sterile lubricating jelly, that a recall has been initiated for this product because the product may be "inadequately sterilized" and use of this product may result in "patient infection". Because this particular sterile lubricating jelly is packaged in the KING LT-D Kit and KING LTS-D Kit, King Systems is sending a Notice of the Reca
Jan 14, 2011	Z-1719-2011	—	terminated	King Systems has been notified by Triad Group, our supplier of sterile lubricating jelly, that a recall has been initiated for this product because the product may be "inadequately sterilized" and use of this product may result in "patient infection". Because this particular sterile lubricating jelly is packaged in the KING LT-D Kit and KING LTS-D Kit, King Systems is sending a Notice of the Reca
Jan 14, 2011	Z-1716-2011	—	terminated	King Systems has been notified by Triad Group, our supplier of sterile lubricating jelly, that a recall has been initiated for this product because the product may be "inadequately sterilized" and use of this product may result in "patient infection". Because this particular sterile lubricating jelly is packaged in the KING LT-D Kit and KING LTS-D Kit, King Systems is sending a Notice of the Reca
Jan 14, 2011	Z-1711-2011	—	terminated	King Systems has been notified by Triad Group, our supplier of sterile lubricating jelly, that a recall has been initiated for this product because the product may be "inadequately sterilized" and use of this product may result in "patient infection". Because this particular sterile lubricating jelly is packaged in the KING LT-D Kit and KING LTS-D Kit, King Systems is sending a Notice of the Reca
Dec 15, 2009	Z-0978-2011	—	terminated	King Systems was issued a warning letter from the Center for Devices and Radiological Health, Office of Compliance on October 28, 2009. The warning letter asserts that Kings Systems KLT(S)-D airway exceeds cleared indications in that it is promoted for "airway management in patients over 4 feet in height, for controlled or spontaneous ventilation, difficult and emergent airway cases, and ambulat
Dec 15, 2009	Z-0986-2011	—	terminated	King Systems was issued a warning letter from the Center for Devices and Radiological Health, Office of Compliance on October 28, 2009. The warning letter asserts that Kings Systems KLT(S)-D airway exceeds cleared indications in that it is promoted for "airway management in patients over 4 feet in height, for controlled or spontaneous ventilation, difficult and emergent airway cases, and ambulat
Dec 15, 2009	Z-0975-2011	—	terminated	King Systems was issued a warning letter from the Center for Devices and Radiological Health, Office of Compliance on October 28, 2009. The warning letter asserts that Kings Systems KLT(S)-D airway exceeds cleared indications in that it is promoted for "airway management in patients over 4 feet in height, for controlled or spontaneous ventilation, difficult and emergent airway cases, and ambulat
Dec 15, 2009	Z-0980-2011	—	terminated	King Systems was issued a warning letter from the Center for Devices and Radiological Health, Office of Compliance on October 28, 2009. The warning letter asserts that Kings Systems KLT(S)-D airway exceeds cleared indications in that it is promoted for "airway management in patients over 4 feet in height, for controlled or spontaneous ventilation, difficult and emergent airway cases, and ambulat
Dec 15, 2009	Z-0976-2011	—	terminated	King Systems was issued a warning letter from the Center for Devices and Radiological Health, Office of Compliance on October 28, 2009. The warning letter asserts that Kings Systems KLT(S)-D airway exceeds cleared indications in that it is promoted for "airway management in patients over 4 feet in height, for controlled or spontaneous ventilation, difficult and emergent airway cases, and ambulat
Dec 15, 2009	Z-0982-2011	—	terminated	King Systems was issued a warning letter from the Center for Devices and Radiological Health, Office of Compliance on October 28, 2009. The warning letter asserts that Kings Systems KLT(S)-D airway exceeds cleared indications in that it is promoted for "airway management in patients over 4 feet in height, for controlled or spontaneous ventilation, difficult and emergent airway cases, and ambulat
Dec 15, 2009	Z-0984-2011	—	terminated	King Systems was issued a warning letter from the Center for Devices and Radiological Health, Office of Compliance on October 28, 2009. The warning letter asserts that Kings Systems KLT(S)-D airway exceeds cleared indications in that it is promoted for "airway management in patients over 4 feet in height, for controlled or spontaneous ventilation, difficult and emergent airway cases, and ambulat
Dec 15, 2009	Z-0985-2011	—	terminated	King Systems was issued a warning letter from the Center for Devices and Radiological Health, Office of Compliance on October 28, 2009. The warning letter asserts that Kings Systems KLT(S)-D airway exceeds cleared indications in that it is promoted for "airway management in patients over 4 feet in height, for controlled or spontaneous ventilation, difficult and emergent airway cases, and ambulat
Dec 15, 2009	Z-0983-2011	—	terminated	King Systems was issued a warning letter from the Center for Devices and Radiological Health, Office of Compliance on October 28, 2009. The warning letter asserts that Kings Systems KLT(S)-D airway exceeds cleared indications in that it is promoted for "airway management in patients over 4 feet in height, for controlled or spontaneous ventilation, difficult and emergent airway cases, and ambulat
Dec 15, 2009	Z-0974-2011	—	terminated	King Systems was issued a warning letter from the Center for Devices and Radiological Health, Office of Compliance on October 28, 2009. The warning letter asserts that Kings Systems KLT(S)-D airway exceeds cleared indications in that it is promoted for "airway management in patients over 4 feet in height, for controlled or spontaneous ventilation, difficult and emergent airway cases, and ambulat
Dec 15, 2009	Z-0977-2011	—	terminated	King Systems was issued a warning letter from the Center for Devices and Radiological Health, Office of Compliance on October 28, 2009. The warning letter asserts that Kings Systems KLT(S)-D airway exceeds cleared indications in that it is promoted for "airway management in patients over 4 feet in height, for controlled or spontaneous ventilation, difficult and emergent airway cases, and ambulat
Dec 15, 2009	Z-0981-2011	—	terminated	King Systems was issued a warning letter from the Center for Devices and Radiological Health, Office of Compliance on October 28, 2009. The warning letter asserts that Kings Systems KLT(S)-D airway exceeds cleared indications in that it is promoted for "airway management in patients over 4 feet in height, for controlled or spontaneous ventilation, difficult and emergent airway cases, and ambulat
Dec 15, 2009	Z-0979-2011	—	terminated	King Systems was issued a warning letter from the Center for Devices and Radiological Health, Office of Compliance on October 28, 2009. The warning letter asserts that Kings Systems KLT(S)-D airway exceeds cleared indications in that it is promoted for "airway management in patients over 4 feet in height, for controlled or spontaneous ventilation, difficult and emergent airway cases, and ambulat
Aug 1, 2008	Z-0789-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0745-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0795-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0809-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0730-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0794-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0721-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0757-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0691-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0701-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0804-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0813-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0685-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0687-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0729-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0734-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0758-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0807-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0696-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0699-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0783-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0816-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0709-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0700-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0714-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0689-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0805-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0812-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0742-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0748-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0796-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0782-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0790-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0736-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0800-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0724-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0683-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0761-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0814-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0682-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0679-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0764-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0681-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0773-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0722-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0740-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0752-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0772-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.
Aug 1, 2008	Z-0785-2009	—	terminated	The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.