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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 13 of 26

Device	Model / Reference	Registries	Class	Status
Circulaire II Aerosol Drug Delivery System	0330	FDA UDI	Class II	Active
Uni-Lim Pressure Plug	8120	FDA UDI	Class I	Active
Disposable Anesthesia Circuit	9362	FDA UDI	Class II	Active
Disposable Respiratory Products, Neo-Pod T	9402U	FDA UDI	Class II	Unknown
Full Kit Pulset™, 1cc Syringe 25g x 5/8" Crickett™ ˜25u BH	3173-91	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	9692	FDA UDI	Class II	Active
Circulaire	0296	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	9342	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	7-8600	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	9573	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	9051	FDA UDI	Class I	Active
CO2/O2 Oral/Nasal Cannula	0915	FDA UDI	Class II	Unknown
MicroBlock	CMI-2711R	FDA UDI	Class II	Active
Uni-Lim 72" Adult Anesthesia Breathing Circuit	8989	FDA UDI	Class II	Active
VixOne Nebulizer	0244	FDA UDI	Class II	Active
Breathing Bag	7-6203	FDA UDI	Class I	Unknown
Adaptors/Connectors	S6260	FDA UDI	Class I	Unknown
UNI-LM Coaxial circuit	9672	FDA UDI	Class II	Active
Disposable anesthesia circuits	9625	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	7-8403-10-62	FDA UDI	Class I	Active
CO2/O2 Nasal Cannula	0916	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuit	9675	FDA UDI	Class I	Active
VixOne	0209	FDA UDI	Class II	Active
Atellica® VTR Syringes	11561347	FDA UDI	Class I	Active
Pulset	3193	FDA UDI	Class I	Unknown
Anesthesia Circuit Kit	R-9203	FDA UDI	Class II	Active
Atellica® VTR Syringes	11561341	FDA UDI	Class I	Active
Face Mask, Large Adult	7-9800	FDA UDI	Class I	Unknown
Comfort Soft Plus	0508	FDA UDI	Class II	Active
Cadwell Sleepmate	302542-200-0484	FDA UDI	Class I	Active
Uni-Lim 60" Adult Anesthesia Circuit	9153	FDA UDI	Class II	Active
Anesthesia Circuit Kit	9806	FDA UDI	Class I	Active
Adult Nasal Cannula for GI Source	08-0004	FDA UDI	Class I	Active
Infant HMEF W/ Sampling Port	6232	FDA UDI	Class II	Active
Mask, Pediatric, Non-Rebreather	3226-E	FDA UDI	Class I	Active
Cord Gas Syringes	3182	FDA UDI	Class I	Unknown
Gas Sampling Line w Reflective Luer	0943	FDA UDI	Class I	Active
Adaptors/Connectors	S6227	FDA UDI	Class I	Active
Hyperinflation AMBU	900 000 628	FDA UDI	Class II	Active
Breathing Bag	BB1000LFB	FDA UDI	Class I	Active
Anesthesia Circuit Kit	R-6882	FDA UDI	Class II	Active
Anesthesia Circuit Kit	9804	FDA UDI	Class I	Active
Bubble Humidifier	0480	FDA UDI	Class I	Active
Accessory Products	9604	FDA UDI	Class I	Active
Anesthesia Circuits	9275	FDA UDI	Class I	Active
Composite Respiratory Kit: Nationwide Medical	0837	FDA UDI	Class I	Active
Hyperinflation AMBU	900 000 617	FDA UDI	Class II	Active
Anesthesia Circuit Kit	R-6884	FDA UDI	Class II	Active
Filter	6159	FDA UDI	Class II	Active
Adapters/Connectors	7-5105	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

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Importers

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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.