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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 10 of 26

Device	Model / Reference	Registries	Class	Status
Tubing	2187	FDA UDI	Class I	Active
Oxygen Tubing, KROT, 21'	0022	FDA UDI	Class I	Unknown
Adaptors/Connectors	0583	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	8624	FDA UDI	Class II	Active
Disposable Anesthesia Circuit Pediatric	9637	FDA UDI	Class I	Active
Disposable Anesthesia Circuit	9322	FDA UDI	Class II	Active
Anesthesia Circuit Kit	R-9426	FDA UDI	Class II	Active
VixOne	0214	FDA UDI	Class II	Active
Blood Gas Sampler	3302-95VT	FDA UDI	Class I	Unknown
Circulaire Aerosol Drug Delivery System	0320	FDA UDI	Class II	Unknown
108" Adult Expandable Anesthesia Circuit	9249	FDA UDI	Class II	Unknown
Disposable Anesthesia Breathing Circuit	8624A	FDA UDI	Class I	Active
Guedel Airways	7-3581	FDA UDI	Class I	Unknown
Pulset	3705	FDA UDI	Class I	Unknown
Comfort Soft Plus CO2 Sampling Nasal Cannula	0539	FDA UDI	Class II	Active
Anesthesia Circuit	9391	FDA UDI	Class II	Active
CO2 Sampling Line	0500	FDA UDI	Class II	Active
Filter	9317	FDA UDI	Class II	Unknown
BlockAide Pulmonary Function Filter	6904-4E	FDA UDI	Class II	Active
Pressure Safe™, CSP	0886	FDA UDI	Class I	Active
Oxygen Tubing, KROT, 40'	0040	FDA UDI	Class I	Active
Hyperinflation	7-N7915-62-29I	FDA UDI	Class II	Active
Mask, Adult Oxygen W/7' KROT	0370	FDA UDI	Class I	Active
Breathing Bag	6395	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuit	622E72G-2N-M2	FDA UDI	Class I	Active
Disposable Anesthesia Circuit	9671	FDA UDI	Class II	Unknown
A-Line Syringe	3100-25	FDA UDI	Class I	Active
Nebulizers	1002222	FDA UDI	Class II	Active
Cadwell Sleepmate	302544-200-0484	FDA UDI	Class I	Active
Uni-Lim, 40" Adult Coaxial Circuit	6651	FDA UDI	Class II	Active
Adult Elongated Non Re breather Mask	3228-E	FDA UDI	Class I	Active
Vibralung Patient Kit	9600-10	FDA UDI	Class II	Active
Filter	A38725HP	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	8042	FDA UDI	Class I	Unknown
Filter	A4091	FDA UDI	Class II	Active
Disposable Breathing Circuits	9216	FDA UDI	Class I	Unknown
IV-Heart™ Continuous Nebulizer	101020	FDA UDI	Class II	Unknown
Transport Kit with Pediatric Elongated Non-Rebrreather Mask with Safety Vent	9443	FDA UDI	Class II	Active
Circuit, Anesthesia, Ped	9561	FDA UDI	Class I	Active
Breathing Bag	7-6205	FDA UDI	Class I	Unknown
Disposable Breathing Circuits	5703	FDA UDI	Class I	Unknown
72" Adult Expandable Anesthesia Circuit	9239	FDA UDI	Class II	Active
Anesthesia Circuit, Pediatric	9581	FDA UDI	Class I	Unknown
Breathing Bag	8841	FDA UDI	Class I	Unknown
Pulset™ 3CC Syringe, 22G X 1"	3302-91	FDA UDI	Class I	Active
Disposable Breathing Circuits	9167	FDA UDI	Class I	Unknown
Hyperinflation	7-N7915-56I-62	FDA UDI	Class II	Active
OxyGo Oxygen Tube	1425-1006	FDA UDI	Class I	Active
Comfort Soft Plus CO2 Sampling Nasal Cannula	0503	FDA UDI	Class II	Active
Anesthesia Circuit Kit	9803	FDA UDI	Class II	Active

Related Companies

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Importers

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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.