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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 11 of 26

Device	Model / Reference	Registries	Class	Status
Disposable Anesthesia Circuits	8856	FDA UDI	Class I	Active
Disposable anesthesia circuits	8029A	FDA UDI	Class II	Active
72' Adult Uni-Lim™ Coaxial Circuit	9247	FDA UDI	Class II	Active
NeoPod "T" 12VDC Power Supply Cable	9400	FDA UDI	Class II	Unknown
Uni-lim Coaxial Circuit	9626	FDA UDI	Class I	Unknown
Comfort Soft Plus CO2/O2 Mask	0562-01	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	8036	FDA UDI	Class II	Active
Comfort Soft Plus	010-105460	FDA UDI	Class I	Active
UnoMist Small Volume Nebulizer	774-E	FDA UDI	Class II	Active
Breathing Circuit	9076	FDA UDI	Class II	Active
Comfort Soft Plus, Infant Soft Tip Cannula	0177	FDA UDI	Class I	Unknown
Hyperinflation (AMBU)	900 000 608	FDA UDI	Class II	Unknown
Adult Soft Tip Cannula (Bulk)	0556B	FDA UDI	Class I	Active
Circulaire II Kit, Hybrid	0399	FDA UDI	Class II	Unknown
Vibralung Mask Interface Kit-Adult with Aerosol Delivery System	9642	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9344	FDA UDI	Class I	Active
Gas Sampling Line With Reflective Luer	0944	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	9295	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	41212-1NV	FDA UDI	Class I	Active
14' Oxygen Tubing	0014B	FDA UDI	Class I	Active
Uni-Lim Coaxial Circuit	9153A	FDA UDI	Class II	Active
Pedi-Lim Coaxial Circuit	9169	FDA UDI	Class I	Active
Gas Sampling Line wit Reflective Luer	0937	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	8029	FDA UDI	Class I	Active
Inline Water Trap	0221B	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9147	FDA UDI	Class I	Unknown
Nebulizer	0205	FDA UDI	Class II	Active
Heart® Direct Connect Cont.Nebulizer, Ped.Super Spike Mask	100628	FDA UDI	Class II	Active
Comfort Soft Plus® CO2 Sampling Nasal Cannula	0913	FDA UDI	Class II	Unknown
InLine Water Trap	1002277	FDA UDI	Class II	Active
A-Line	3300-24	FDA UDI	Class I	Active
Heart® Continuous Nebulizer Holder	100950	FDA UDI	Class II	Unknown
Anesthesia Circuit Kit	R-9421	FDA UDI	Class II	Active
Comfort Soft Plus	0566-RC	FDA UDI	Class I	Unknown
Adaptors/Connectors	7-SP5088	FDA UDI	Class I	Unknown
Super Spike Aerosol Masks	0375	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	8075	FDA UDI	Class II	Active
BagEasy	562111	FDA UDI	Class II	Unknown
Oxygen Mask	0371	FDA UDI	Class I	Active
OxyGo Adult Cannula	1425-1001	FDA UDI	Class I	Active
Cannula, Adult, Soft Tip, W/14' KROT	0198	FDA UDI	Class I	Active
Blood Gas Sampler	3303-94	FDA UDI	Class I	Unknown
Atellica® VTR Syringes	11561340	FDA UDI	Class I	Active
Atellica® VTR Syringes	11561345	FDA UDI	Class I	Active
Adult Venturi Elongated Mask Kit	3120-E	FDA UDI	Class I	Active
Vibralung®	9500D	FDA UDI	Class II	Active
Anesthesia Circuit Kit	9811	FDA UDI	Class I	Active
Aerosol Masks	0301	FDA UDI	Class I	Unknown
CO2 Easy	562134	FDA UDI	Class II	Active
Pulset	3303+	FDA UDI	Class II	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.