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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 3 of 26

Device	Model / Reference	Registries	Class	Status
Circulaire II Hybrid Aerosol Drug Delivery System	0393R	FDA UDI	Class II	Active
Pulset	3303-95	FDA UDI	Class I	Unknown
Adult CO2/O2 Cannula	2101-W	FDA UDI	Class II	Active
Co2/O2 Oral/Nasal Cannula	0921	FDA UDI	Class I	Unknown
Non-Rebreather Mask	0366	FDA UDI	Class I	Active
Disposable Anesthesia Circuit	9679	FDA UDI	Class II	Unknown
Adaptor/Connector	010-105528	FDA UDI	Class I	Active
Adaptors/Connectors	S3000	FDA UDI	Class I	Unknown
Anapod Controller	A2003R	FDA UDI	Class II	Unknown
Hme	6229	FDA UDI	Class II	Unknown
Neo-Pod T Circuit	9399	FDA UDI	Class II	Unknown
Anesthesia Circuit, Adult, Uni-Lim, 60"	9262	FDA UDI	Class I	Active
Hyperinflation (ABMU)	900 000 611	FDA UDI	Class II	Active
BagEasy	562200	FDA UDI	Class II	Unknown
Biflo Nasal Mask	0101	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	7-8901-10-69	FDA UDI	Class I	Active
Mask	1002230	FDA UDI	Class I	Active
Adaptors/Connectors	S6261	FDA UDI	Class I	Unknown
96`Adult Anesthesia Expandable Circuit	8035	FDA UDI	Class I	Active
BlockAide Pulmonary Function Filter	6901-1R	FDA UDI	Class II	Active
Anesthesia/Breathing Circuits	9701	FDA UDI	Class II	Unknown
Ventilator Circuit, Neonatal, 50'	N6205CKT	FDA UDI	Class I	Active
Adult circuit, 120" Expandable Tubing	9632	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	7-8413-10-62	FDA UDI	Class I	Active
BagEasy	562086	FDA UDI	Class II	Unknown
OxyGo Adult Nasal Cannula with Straight Tip	1425-1003	FDA UDI	Class I	Active
Heart® Continuous Nebulizer, Pediatric Kit	100649	FDA UDI	Class II	Unknown
96" Anesthesia Circuit	9435	FDA UDI	Class I	Active
Syringe	3314	FDA UDI	Class I	Unknown
Anesthesia Circuit Kit	9802	FDA UDI	Class II	Active
CO2/O2 Nasal Cannula	0920	FDA UDI	Class I	Unknown
NeoPod	9437	FDA UDI	Class II	Unknown
BagEasy	562236	FDA UDI	Class II	Active
Adult Face Tent	0355	FDA UDI	Class I	Active
Pulset	3193CH	FDA UDI	Class I	Unknown
Flex Hose	0470	FDA UDI	Class I	Active
Anesthesia Circuit Kit	R-9338	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	8822	FDA UDI	Class I	Active
Adult Nasal Cannula for GI Source	08-0002	FDA UDI	Class I	Active
CO2 Sampling Nasal Cannula	0534	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9422	FDA UDI	Class I	Unknown
Capette	CP-4203	FDA UDI	Class I	Active
Controllers/Accessories	4056	FDA UDI	Class II	Unknown
AnaPod	A2003	FDA UDI	Class II	Unknown
Adult Nasal Cannula for GI Source	08-0005	FDA UDI	Class I	Active
Disposable anesthesia circuits	9596	FDA UDI	Class I	Active
Anesthesia Circuit Kit	R-8264	FDA UDI	Class II	Active
Pulset	3600	FDA UDI	Class I	Active
60" Adult Anesthesia Circuit	9158	FDA UDI	Class II	Active
Oxygen Tubing, 7' KROT, w/ (2) Long Straights	0007	FDA UDI	Class I	Unknown

Related Companies

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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.