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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 15 of 26

Device	Model / Reference	Registries	Class	Status
Disposable Anesthesia Circuits	9104	FDA UDI	Class II	Active
Disposable Anesthesia Circuit	8310	FDA UDI	Class I	Active
Comfort Soft Plus® Cannula	0586	FDA UDI	Class I	Active
Mask	1002220	FDA UDI	Class I	Active
Cadwell Sleepmate	302545-200-0484	FDA UDI	Class I	Active
Disposable Breathing Circuits	6368	FDA UDI	Class I	Active
Hyperinflation AMBU	900 000 623	FDA UDI	Class II	Unknown
Hyperinflation	0414	FDA UDI	Class II	Active
Composite Respiratory Kit	0798	FDA UDI	Class II	Active
Dynaris Cannula Assembly 3'	902028	FDA UDI	Class I	Active
Disposable Heated Humidified Circuit Kit	9657	FDA UDI	Class I	Active
Disposable Anesthesia Circuit	6788	FDA UDI	Class I	Active
Nasal Mask, Pediatric	0106	FDA UDI	Class I	Active
Nebulizers	1002225	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	8270	FDA UDI	Class I	Active
Comfort Soft Plus CO2 Sampling Nasal Cannula	0584	FDA UDI	Class I	Active
Dynaris Demand Cannula Assembly	902024	FDA UDI	Class I	Active
Anesthesia Circuit	8141	FDA UDI	Class II	Active
MicroBlock	CMI-2715R	FDA UDI	Class II	Active
Hyperinflation (AMBU)	900 000 603	FDA UDI	Class II	Active
96" Adult Expandable Anesthesia Circuit	9246	FDA UDI	Class II	Active
CO2/O2 Nasal Cannula	0914	FDA UDI	Class II	Unknown
Gas Sampling Line	0903	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9074	FDA UDI	Class II	Active
UnoMist™ Small Volume Nebulizer	3778-E	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	M436F3C11J000	FDA UDI	Class II	Active
AMBU Co2 Detector-Pedi	000-172-713	FDA UDI	Class II	Active
Anesthesia Mask	7-9904	FDA UDI	Class I	Unknown
Oxygen Tubing, KROT, 50'	0050	FDA UDI	Class I	Active
Uni-Lim Circuit	9139	FDA UDI	Class I	Active
FloEasy Co-Flo	9570	FDA UDI	Class I	Unknown
Cannula, Adult Nasal, soft tipped, w/4' KROT	0194	FDA UDI	Class I	Unknown
Adult Uni-Lim™ Circuit	9578	FDA UDI	Class II	Active
Comfort Soft Plus	0430	FDA UDI	Class I	Active
AMBU Co2 Detector	000-172-714	FDA UDI	Class II	Active
Infant Oxygen Mask	3262-E	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	7-7102-66	FDA UDI	Class I	Unknown
Heart® Direct Connect Continuous Nebulizer, Adult Kit	100619	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9302	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	8024	FDA UDI	Class I	Active
Pressure Safe™ CSP	0887	FDA UDI	Class I	Active
Disposable Respiratory Circuit	7-SP5651	FDA UDI	Class I	Active
Comfort Soft Plus CO2 Sampling Nasal Cannula	0542	FDA UDI	Class II	Active
Heated Circuit	9313	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9276	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	7-SP5659	FDA UDI	Class II	Active
Disposable Anesthesia Circuit	9636	FDA UDI	Class I	Active
Adaptors/Connectors	6588	FDA UDI	Class I	Unknown
Comfort Soft Plus Cannula High Flow	0569	FDA UDI	Class I	Active
Disposable anesthesia circuits	9594	FDA UDI	Class I	Active

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.