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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 25 of 26

Device	Model / Reference	Registries	Class	Status
Vibralung Patient Change Kit	9640	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	N1332	FDA UDI	Class I	Unknown
A-Line	3300-25VT	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	8970	FDA UDI	Class I	Active
Heart® Continuous Nebulizer	100609	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9063	FDA UDI	Class II	Unknown
BagEasy	562080	FDA UDI	Class II	Unknown
UNI-LIM Coaxial Circuit	8102	FDA UDI	Class I	Active
Transport Set	6214	FDA UDI	Class II	Active
Disposable Anesthesia Circuit	9360	FDA UDI	Class II	Active
Atellica® VTR Syringes	11561346	FDA UDI	Class II	Active
Disposable Breathing Circuits	9419	FDA UDI	Class I	Unknown
Pulset™ 1cc Syringe	3100	FDA UDI	Class I	Active
Anti-Drool Tee	0245	FDA UDI	Class I	Active
Muc-Away™	0492	FDA UDI	Class II	Active
NeoPod "T" AC to DC Power Supply Cable	9401R	FDA UDI	Class II	Active
Circulaire Aerosol Drug Delivery System	0260	FDA UDI	Class II	Unknown
Disposable Respiratory Circuits	6513	FDA UDI	Class II	Active
Hyperinflation AMBU	900 000 624	FDA UDI	Class II	Active
Hyperinflation	7-N7905-N-MAN	FDA UDI	Class II	Active
Adult Cannula, Conventional w/7' Kink Resistant Tubing	0107	FDA UDI	Class I	Unknown
Pedi-Neb Nasal Nebulizer	0382	FDA UDI	Class II	Active
Uni-Lim 60" Adult Coaxial Circuit	8606	FDA UDI	Class I	Active
Blood Gas Sampler	ABG-3603-VS	FDA UDI	Class I	Active
Microspacer, Bulk	THS-BMS	FDA UDI	Class II	Active
MicroBlock	CMI-2713R	FDA UDI	Class II	Active
Uni-Lim 60" Anesthesia Breathing Circuit	9061	FDA UDI	Class II	Active
Pro-Nox	WES-PROLRGKIT	FDA UDI	Class I	Active
Gas Sampling Line	0513	FDA UDI	Class I	Active
Pulset	3302+	FDA UDI	Class II	Active
Elongated Aerosol Mask	100-E	FDA UDI	Class I	Active
Uni-Lim 72" Adult Coaxial Breathing Circuit	8048	FDA UDI	Class II	Active
Atellica® VTR Syringes	11561344	FDA UDI	Class I	Active
Uni-Lim Coaxial Circuit	6654	FDA UDI	Class I	Active
Uni-Lim Coaxial Circuit	9416	FDA UDI	Class I	Active
Pulset	3373	FDA UDI	Class I	Unknown
Hyperinflation	900 000 621	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	8866	FDA UDI	Class II	Active
Berman Oral Airway	1002266	FDA UDI	Class I	Active
Septal-H Infant Size	CP-5500A	FDA UDI	Class I	Active
Anesthesia Mask	7-9901	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	5705 MX	FDA UDI	Class I	Active
Breathing Bag	6393	FDA UDI	Class I	Unknown
Vibralung Treatment Control Unit	9500	FDA UDI	Class II	Active
Pulset	3703-91	FDA UDI	Class I	Active
Adult CO2 /O2 Mask	0931	FDA UDI	Class I	Unknown
144" Expandable Adult Anesthesia Circuit	9203	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	9323	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	9284	FDA UDI	Class II	Unknown
Tubing	2189	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

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.