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WESTMED, INC.

Last updated September 17, 2026

Information

Country: US
Address: 5580 S NOGALES HWY, TUCSON, AZ, 85706
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 1000374126
DUNS Number: 092673953

Catalogue (1289)

Page 17 of 26

Device	Model / Reference	Registries	Class	Status
CO2 Easy	562135	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9274	FDA UDI	Class II	Active
Concentrator Humidifier Adapter	0485B	FDA UDI	Class I	Active
Uni-Lim 96" Anesthesia Circuit	9336	FDA UDI	Class I	Active
Comfort Soft Plus CO2 Sampling Nasal Cannula	0538	FDA UDI	Class II	Active
Anesthesia Circuit Kit	9801	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9681	FDA UDI	Class I	Unknown
Uni-Lim 72" Anesthesia Circuit	8041	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9392	FDA UDI	Class I	Active
Adult Comfort Plus	0715	FDA UDI	Class I	Unknown
Face Mask, Infant	7-9804	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	9575	FDA UDI	Class I	Active
Berman Oral Airway	1002265	FDA UDI	Class I	Active
Uni-Lim Coaxial Breathing Circuit	9634	FDA UDI	Class I	Active
Disposable Heated Humidified Circuit Kit	9658	FDA UDI	Class I	Active
72' 28V Adult HW Circuit, PAR WYE, Water, BV Filter, Water Trap	9240	FDA UDI	Class I	Unknown
Composite Respiratory Kit- Medical West	0713	FDA UDI	Class II	Active
CO2 Sampling Nasal Cannula	0874	FDA UDI	Class I	Unknown
Composite Kit	0793	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	7-8103-10-68	FDA UDI	Class I	Active
Tubing	0472	FDA UDI	Class I	Unknown
Variable Pressure Safe™ Infant Nasal Cannula	0879	FDA UDI	Class I	Unknown
WaterPAP	WP-7700	FDA UDI	Class II	Active
Disposable Anesthesia Circuit	9014	FDA UDI	Class I	Active
Oxygen Tubing Swivel Connector, bulk	0590B	FDA UDI	Class I	Active
Circulaire II PEP Accessory Kit	0338	FDA UDI	Class II	Unknown
Transport Kit with Infant Elongated Oxygen Mask	9441	FDA UDI	Class II	Active
Pedi-Lim Breathing Circuit	9060	FDA UDI	Class II	Active
Comfort Soft Plus Cannula High Flow	0558	FDA UDI	Class I	Active
CO2 Sampling Nasal Cannula	0505-01	FDA UDI	Class II	Active
Circulaire II PEP Accessory Kit	0337	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	7-9201-10-62	FDA UDI	Class I	Active
CO2 Sampling Nasal Cannula 72` w/Female Luer	0872	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	9341	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	7-8100	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	8105	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	7-8113-10-67	FDA UDI	Class II	Active
Hyperinflation	7-N7905-I-MAN	FDA UDI	Class II	Active
Comfort Soft Plus	1002344	FDA UDI	Class I	Active
Anesthesia Circuit	9364	FDA UDI	Class II	Active
Uni-Lim 72" Adult Coaxail Breathing Circuit	9242	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	7-8000	FDA UDI	Class I	Active
Disposable Anesthesia Circuit	9676	FDA UDI	Class II	Active
Disposable Anesthesia Breathing Circuits	6619	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuit	6880	FDA UDI	Class I	Active
Oxygen Tubing	0004-50	FDA UDI	Class I	Unknown
VixOne™ Reusable Nebulizer	0397	FDA UDI	Class II	Active
Comfort Soft Plus Cannula High Flow	0557	FDA UDI	Class I	Active
Gas Sampling Line	0511	FDA UDI	Class I	Unknown
Uni-Lim 40" Anesthesia Breathing Circuit	8004	FDA UDI	Class II	Unknown

Related Companies

Authorised Representatives

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Importers

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Notified Bodies

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Authorities

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FDA Recalls (26)

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
Sep 27, 2024	Z-0263-2025	—	open, classified	Due to connector within the circuit flex extender not meeting specifications resulting in a low connection force and as a result, the connector may leak or disconnect and may cause life threating conditions or death.
Nov 11, 2020	Z-0746-2021	—	terminated	There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection to the mask adapter resulting in a possible delay in treatment.
Nov 11, 2020	Z-0743-2021	—	terminated	There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection to the mask adapter resulting in a possible delay in treatment.
Nov 11, 2020	Z-0741-2021	—	terminated	There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection to the mask adapter resulting in a possible delay in treatment.
Nov 11, 2020	Z-0742-2021	—	terminated	There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection to the mask adapter resulting in a possible delay in treatment.
Nov 11, 2020	Z-0744-2021	—	terminated	There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection to the mask adapter resulting in a possible delay in treatment.
Nov 11, 2020	Z-0745-2021	—	terminated	There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection to the mask adapter resulting in a possible delay in treatment.
Jan 15, 2019	Z-2436-2020	—	terminated	A repair was made to an adapter mold resulting in parts being produced with compliant 10mm ID connections and non-compliant 15mm OD connections. This resulted in facilities with infant resuscitators that connect via the 15mm OD fitting not being able to use those circuits.
Jan 15, 2019	Z-2434-2020	—	terminated	A repair was made to an adapter mold resulting in parts being produced with compliant 10mm ID connections and non-compliant 15mm OD connections. This resulted in facilities with infant resuscitators that connect via the 15mm OD fitting not being able to use those circuits.
Jan 15, 2019	Z-2435-2020	—	terminated	A repair was made to an adapter mold resulting in parts being produced with compliant 10mm ID connections and non-compliant 15mm OD connections. This resulted in facilities with infant resuscitators that connect via the 15mm OD fitting not being able to use those circuits.
Jan 18, 2011	Z-0104-2013	—	terminated	Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential contaminants.
Jan 18, 2011	Z-0108-2013	—	terminated	Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential contaminants.
Jan 18, 2011	Z-0101-2013	—	terminated	Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential contaminants.
Jan 18, 2011	Z-0100-2013	—	terminated	Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential contaminants.
Jan 18, 2011	Z-0097-2013	—	terminated	Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential contaminants.
Jan 18, 2011	Z-0106-2013	—	terminated	Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential contaminants.
Jan 18, 2011	Z-0109-2013	—	terminated	Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential contaminants.
Jan 18, 2011	Z-0098-2013	—	terminated	Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential contaminants.
Jan 18, 2011	Z-0096-2013	—	terminated	Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential contaminants.
Jan 18, 2011	Z-0105-2013	—	terminated	Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential contaminants.
Jan 18, 2011	Z-0107-2013	—	terminated	Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential contaminants.
Jan 18, 2011	Z-0102-2013	—	terminated	Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential contaminants.
Jan 18, 2011	Z-0103-2013	—	terminated	Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential contaminants.
Jan 18, 2011	Z-0099-2013	—	terminated	Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential contaminants.
Jun 22, 2010	Z-2333-2010	—	terminated	This recall was initiated after Westmed, Inc. became aware of a potential for disconnection at the patient port retention ring assembly of the Bag Easy manual resuscitation device.
Jun 22, 2010	Z-2332-2010	—	terminated	This recall was initiated after Westmed, Inc. became aware of a potential for disconnection at the patient port retention ring assembly of the Bag Easy manual resuscitation device.