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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 4 of 26

Device	Model / Reference	Registries	Class	Status
Adult Heated Wick Circuit	A9240SS	FDA UDI	Class II	Unknown
BlockAide Pulmonary Function Filter	6902-2E	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	7-8113-10	FDA UDI	Class I	Active
Disposable anesthesia circuits, Adult 40"	8253	FDA UDI	Class II	Active
Hyperinflation (AMBU)	900 000 607	FDA UDI	Class II	Unknown
Comfort Soft Plus, Neonatal	0163	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	7-7105-66	FDA UDI	Class I	Unknown
Flex Extenders	2179	FDA UDI	Class I	Unknown
Test Lung 1L	6012	FDA UDI	Class I	Unknown
Anesthesia/Breathing Circuits	8167	FDA UDI	Class II	Unknown
Tubing	0469	FDA UDI	Class I	Unknown
Disposable Breathing Circuits	9404	FDA UDI	Class I	Unknown
CO2 Sampling Nasal Cannula	2100-50	FDA UDI	Class II	Active
Comfort Soft Plus, Premature	0153	FDA UDI	Class I	Unknown
Disposable Respiratory Circuits	9289	FDA UDI	Class I	Unknown
NeoPod `T` Transport Controller, W/Pole mounting bracket	4006-1R	FDA UDI	Class II	Active
MicroBlock	CMI-2712R	FDA UDI	Class II	Active
Uni-Lim Coaxial Circuit	8126	FDA UDI	Class I	Active
CO2/O2 Oral/Nasal Cannula	0918	FDA UDI	Class II	Unknown
Pulset	3163-95	FDA UDI	Class I	Unknown
Blood Gas Sampler	3105-94	FDA UDI	Class I	Unknown
Atellica® VTR Syringes	11561350	FDA UDI	Class II	Active
Anapod™ Humi-therm Heated and Humidified Wick Breathing Circuit	A9242	FDA UDI	Class II	Active
Face Mask, Large Adult	7-9810	FDA UDI	Class I	Active
Comfort Soft Plus CO2/O2 Mask	0562	FDA UDI	Class I	Active
Atellica® VTR Syringes	11561348	FDA UDI	Class II	Active
Face Mask, Small Adult	7-9802	FDA UDI	Class I	Unknown
CO2 Sampling Nasal Cannula	0501	FDA UDI	Class II	Active
Replacement Cabel for ANAPOD	A4072	FDA UDI	Class II	Unknown
Cadwell Sleepmate	302572-200-0484	FDA UDI	Class II	Active
Pediatric Expandable Circuit	9006	FDA UDI	Class I	Unknown
Hyperinflation AMBU	900 000 626	FDA UDI	Class II	Unknown
FloEasy	9572HTS	FDA UDI	Class II	Unknown
Adaptors/Connectors	S6420P	FDA UDI	Class I	Active
Circulaire	0290	FDA UDI	Class I	Active
Cannula, Adult High Flow	0554	FDA UDI	Class I	Active
BagEasy	562111DM	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	7-9201-10	FDA UDI	Class I	Active
Aerosol Masks	220-E	FDA UDI	Class I	Active
Guedel Airway	7-3561	FDA UDI	Class I	Unknown
Uni-Lim 72" Adult Coaxail Breathing Circuit	8994	FDA UDI	Class II	Unknown
Medium Adult Anesthesia Mask	7-7701	FDA UDI	Class I	Unknown
Atellica® VTR Syringes	11561351	FDA UDI	Class II	Active
Disposable Anesthesia Breathing Circuits	9129	FDA UDI	Class I	Active
Anesthesia Circuit	8267	FDA UDI	Class II	Unknown
Guedel Oral Airway	7-4051	FDA UDI	Class I	Unknown
Guedel Airways	7-3591	FDA UDI	Class I	Unknown
Gas Sampling Line With Reflective Luer	0938	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	61260T	FDA UDI	Class II	Active
Oxygen Tubing, KROT, 50', Green	0052	FDA UDI	Class I	Unknown

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.