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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 14 of 26

Device	Model / Reference	Registries	Class	Status
OxyGo Swivel Connector	1425-1012	FDA UDI	Class I	Active
Pulset	3372	FDA UDI	Class I	Active
BlockAide Pulmonary Function Filter	6905-5E	FDA UDI	Class II	Active
Circulaire II Aerosol Delivery System	0332	FDA UDI	Class II	Active
Circulaire II Hybrid Aerosol Drug Delivery System	0391R	FDA UDI	Class II	Unknown
72` 28V Adult HW Circuit, PAR WYE	A9240	FDA UDI	Class II	Active
A-Line	3100-30	FDA UDI	Class I	Active
Disposable Anesthesia Circuit	9628	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	8592	FDA UDI	Class II	Unknown
Filter	A38485HP	FDA UDI	Class II	Unknown
MicroBlock	CMI-2715E	FDA UDI	Class II	Active
AnaPod	A4071	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	8533	FDA UDI	Class II	Active
Comfort Soft Plus™ Adult Nasal Cannula, Soft-tipped, w/25'KROT	0537	FDA UDI	Class I	Unknown
Vibralung Full User Kit/Travel Bag	9501	FDA UDI	Class II	Active
Anesthesia Coaxial Circuit	7-6800	FDA UDI	Class I	Active
Connector, Oxygen Swivel	0590	FDA UDI	Class I	Unknown
A-Line	3333-95	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	7-7103-66	FDA UDI	Class I	Unknown
BagEasy	562133	FDA UDI	Class II	Unknown
Uni-Lim 60" Anesthesia Breathing Circuit	9079	FDA UDI	Class I	Active
Comfort Soft Plus, Pediatric Soft Tip Cannula	0187	FDA UDI	Class I	Unknown
Pulset	3372-95	FDA UDI	Class I	Unknown
Filter	6221	FDA UDI	Class II	Active
Anesthesia/Breathing Circuits	9700	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	9053	FDA UDI	Class I	Active
Composite Kit	0792	FDA UDI	Class II	Active
Adult Elongated Non-Rebreather Mask w/o Safety Valve	3108-E	FDA UDI	Class I	Active
BagEasy	562235	FDA UDI	Class II	Unknown
Uni-Heart™ Lo-Flo Continuous Nebulizer, Pediatric Mask, 7'	100941	FDA UDI	Class II	Unknown
Vibralung Mask Interface Kit-Pediatric w/Aerosol Delivery System	9643	FDA UDI	Class II	Active
Oxygen Tubing	1002243	FDA UDI	Class I	Active
72" Adult Anesthesia Circuit	9165	FDA UDI	Class I	Active
Comfort Soft Plus Cannula High Flow	0559	FDA UDI	Class I	Active
Disposable Anesthesia Breathing Circuits	8010	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	8677	FDA UDI	Class I	Unknown
Cannula, Adult, Soft Tip, W/25' KROT	0195	FDA UDI	Class I	Active
Adult Nasal Cannula	0716	FDA UDI	Class I	Unknown
Composite Respiratory Kit: A&R Medical	0758	FDA UDI	Class II	Active
Adaptors/Connectors	S6411P	FDA UDI	Class I	Active
OxyGo Oxygen Tubing	1425-1007	FDA UDI	Class I	Active
Uni-Lim Coaxial Circuit	9694	FDA UDI	Class II	Active
Anesthesia Mask, Large Adult	6384	FDA UDI	Class I	Unknown
Controllers/Accessories	4350	FDA UDI	Class II	Unknown
Gas Sampling Line	0950	FDA UDI	Class I	Unknown
Hyperinflation (AMBU)	900 000 605	FDA UDI	Class II	Active
BagEasy	562040	FDA UDI	Class II	Unknown
VixOne	0236	FDA UDI	Class II	Unknown
Breathing Bag	7-6202	FDA UDI	Class I	Unknown
AnaPod	A4070	FDA UDI	Class II	Unknown

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.