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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 12 of 26

Device	Model / Reference	Registries	Class	Status
Pulset	3313-91	FDA UDI	Class I	Active
OxyGo Oxygen Mask	1425-1010	FDA UDI	Class I	Active
Composite Respiratory Kit	0799	FDA UDI	Class II	Active
Oxygen Tubing	1002279	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	8661	FDA UDI	Class II	Active
Anesthesia Circuit Kit	9810	FDA UDI	Class I	Active
Air Cylinder Wrench	0700	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	8328	FDA UDI	Class II	Unknown
Heart® Continuous Nebulizer Adult Kit, 10cc Syringe	100626	FDA UDI	Class II	Active
Nebulizer	0254	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9338	FDA UDI	Class I	Active
Anapod	A2003-1	FDA UDI	Class II	Unknown
Bubble Humidifier	0795	FDA UDI	Class I	Active
MR Patient Care LoFlo Sample Line, Adult Cannula, Box 20	P183241	FDA UDI	Class II	Active
Non-Rebreather Mask with GSL	0364	FDA UDI	Class II	Unknown
Oxygen Tubing, 25' (GREEN) KROT	0027	FDA UDI	Class I	Active
IV-Heart™ Continuous Nebulizer Adult Kit	101021	FDA UDI	Class II	Unknown
Anesthesia Circuit Kit	R-9274	FDA UDI	Class II	Active
Pulset	3312-95	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	8601	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	9270	FDA UDI	Class I	Active
Vibralung Battery Charger	9630	FDA UDI	Class II	Active
Capette	CP-4403	FDA UDI	Class I	Active
Pulset	3600-30	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	9324	FDA UDI	Class I	Unknown
Anesthesia Circuit Kit	R-9104	FDA UDI	Class II	Active
HME Filter	1002258	FDA UDI	Class I	Active
MADA Medical Cannula, Adult Nasal, Soft Tip, W/7' KROT	1325-7	FDA UDI	Class I	Unknown
BagEasy	562201	FDA UDI	Class II	Active
CO2 Sampling Nasal Cannula 72` w/Male Luer	0871	FDA UDI	Class II	Unknown
Comfort Soft Plus CO2 Sampling Nasal Cannula	0585	FDA UDI	Class I	Unknown
Pulset™ 3CC Syringe, A-Line, Blunt Tip w/protective sheath, 25 U BH	3300-31	FDA UDI	Class I	Active
VixOne	0211	FDA UDI	Class II	Active
Hyperinflation AMBU	900 000 614	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9064	FDA UDI	Class II	Active
Disposable PEP Devices	0262	FDA UDI	Class II	Active
Connector, Oxygen Swivel w/Male and Female ends	0593	FDA UDI	Class I	Unknown
Co-Flo Heated Humidified Circuit	9586	FDA UDI	Class II	Active
Circulaire® Mask - Pediatric Aerosol, Non-Vented	0291	FDA UDI	Class I	Active
Uni-Lim™ Coaxial Circuit	8809-W	FDA UDI	Class I	Active
Comfort Soft Plus	1002348	FDA UDI	Class I	Active
Oxygen Tubing, KROT, 25' Clear	0025	FDA UDI	Class I	Unknown
VixOne Nebulizer	0327	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	7-8103-10	FDA UDI	Class I	Active
MicroBlock	CMI-2714R	FDA UDI	Class II	Active
Uni-Lim Coaxial Circuit	9695	FDA UDI	Class II	Unknown
Humidifier Adaptor	0485	FDA UDI	Class I	Active
Disposable Anesthesia Circuit	9576	FDA UDI	Class II	Active
Pro-Nox	WES-PROSMLKIT	FDA UDI	Class I	Active
FloEasy	9571HTS	FDA UDI	Class I	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.