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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 7 of 26

Device	Model / Reference	Registries	Class	Status
Adapters/Connectors	7-5122	FDA UDI	Class I	Active
MR Patient Care Adult LoFLo CO2 with O2 Cannulas (100)	P185361	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	8329	FDA UDI	Class II	Active
Anesthesia services and products Inc.	AC6616	FDA UDI	Class II	Unknown
Pedi-lim Coaxial Circuit	9414	FDA UDI	Class I	Active
Pulset	3373-95	FDA UDI	Class I	Unknown
Pulset	3183	FDA UDI	Class I	Unknown
Disposable Respiratory Circuits	9693	FDA UDI	Class II	Unknown
Cord Gas Kit	3182-91	FDA UDI	Class I	Active
OxyGo Adult Cannula	1425-1000	FDA UDI	Class I	Active
Face Mask, Neonatal	7-9805	FDA UDI	Class I	Active
Gas Sampling Line With Filter	A9250	FDA UDI	Class I	Active
Pedi-lim Coaxial Circuit	9413	FDA UDI	Class I	Active
72" Adult Anesthesia Circuit	9135	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9426	FDA UDI	Class I	Active
Adaptors/Conectors	20843882	FDA UDI	Class I	Active
Pressure Safe	9655PS	FDA UDI	Class II	Active
Adult High Flow Cannula	0548	FDA UDI	Class I	Active
Face Mask, Medium Adult	7-9811	FDA UDI	Class I	Active
Ambu Hyper System	600 000 615	FDA UDI	Class II	Active
Nebulizer Compressor Filter	6313	FDA UDI	Class II	Active
A-Line	3500-25	FDA UDI	Class I	Active
Vortran PercussiveNeb 2.0	8030	FDA UDI	Class I	Active
UnoMist™ Nebulizer Mask Kit	3776-E	FDA UDI	Class II	Unknown
Hyperinflation	900 000 622	FDA UDI	Class II	Unknown
Comfort Soft Plus	010-0556	FDA UDI	Class I	Active
Anesthesia Mask	7-9903	FDA UDI	Class I	Unknown
Pulset	3322-95	FDA UDI	Class I	Unknown
Comfort Soft Plus® Adult Cannula High Flow	0551-TN	FDA UDI	Class I	Active
Disposable Anesthesia Breathing Circuits	8095	FDA UDI	Class I	Unknown
Adaptor	7-5117	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	8819	FDA UDI	Class II	Unknown
Oxygen Tubing, 7' KROT, w/Threaded Nut (S)	0008	FDA UDI	Class I	Unknown
Cannula, Adult Nasal, Soft Tip, W/14' KROT & Threaded Nut	0199	FDA UDI	Class I	Unknown
Pulset	3702	FDA UDI	Class I	Unknown
Pediatric Elongated Medium Concentration Mask w/8' Tubing, TN	3222-E	FDA UDI	Class I	Active
Hyperinflation	0413	FDA UDI	Class II	Active
Anapod	A2003-1R	FDA UDI	Class II	Unknown
Anesthesia/Breathing Circuits	9394	FDA UDI	Class I	Active
Comfort Soft Plus CO2 Sampling Nasal Cannula	0503F	FDA UDI	Class II	Active
MR Patient Care LoFlo CO2 with Airway Adapters (100)	P185381	FDA UDI	Class I	Active
Disposable Anesthesia Circuit	9678	FDA UDI	Class I	Unknown
Pulset	3103+	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	8569	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9434	FDA UDI	Class II	Active
Adult Expandable Circuit	9004	FDA UDI	Class I	Unknown
Mod Kit Pulset™	3362-91	FDA UDI	Class I	Active
Controllers/Accessories	4357	FDA UDI	Class II	Active
Oxygen Tubing	1002239	FDA UDI	Class I	Active
Mask	1002249	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

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.