Is this your brand? Sign in to claim ownership.

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 6 of 26

Device	Model / Reference	Registries	Class	Status
Nebulizer	0325	FDA UDI	Class II	Active
Uni-lim Coaxial Circuit	6888	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9280	FDA UDI	Class I	Active
Gas Sampling Line	0517	FDA UDI	Class I	Active
MicroBlock	CMI-2712E	FDA UDI	Class II	Active
Filter	A4334	FDA UDI	Class II	Unknown
CSP Elongated Non-Rebreather Mask	0368	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	9417	FDA UDI	Class I	Active
Hyperinflation	7-N7910	FDA UDI	Class II	Active
Comfort Soft Plus, Premature Soft Tipped Cannula	0152	FDA UDI	Class I	Unknown
Composite Respiratory Kit	0767	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	7-8912-10-69-H	FDA UDI	Class II	Active
MicroBlock	CMI-2716R	FDA UDI	Class II	Active
Septal-H	CP-5410	FDA UDI	Class I	Active
Neo-Vent Infant T-Piece Resuscitation Circuit w/Neonatal Mask	0421	FDA UDI	Class II	Unknown
VixOne	0217	FDA UDI	Class II	Active
Anesthesia Circuit Kit	R-9148	FDA UDI	Class II	Active
Disposable Anesthesia Circuit	9659	FDA UDI	Class II	Unknown
OxyGo Comfort Soft Plus® Adult Cannula	1425-1005	FDA UDI	Class I	Active
Anesthesia Mask	7-9900	FDA UDI	Class I	Active
Adult Nasal Cannula, Bulk	0194B	FDA UDI	Class I	Active
Adult Nasal Cannula for GI Source	08-0007	FDA UDI	Class I	Active
Pulset Syringe with Sheathed Blunt Tip Cannula	3100-31	FDA UDI	Class I	Active
Filter	6379	FDA UDI	Class II	Active
Anesthesia Mask	7-9801	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	8279	FDA UDI	Class I	Unknown
CO2/O2 Nasal Cannula	0919	FDA UDI	Class I	Unknown
Oxygen Tubing, KROT, 50', Purple	0055	FDA UDI	Class I	Unknown
96" Anesthesia Circuit	9685	FDA UDI	Class I	Unknown
Composite Respiratory Kit - Medical West	0712	FDA UDI	Class II	Active
Comfort Soft Plus CO2 Sampling Nasal Cannula	0504	FDA UDI	Class I	Active
Disposable Respiratory Circuits	6754	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	8019	FDA UDI	Class II	Active
Disposable Anesthesia Circuit	9663	FDA UDI	Class II	Active
Pulset™ 3cc Syringe 23g x 1" Safety Tip™ ˜25u BH (0.6 x 25mm)	3343-91	FDA UDI	Class I	Active
Ambu Hyper System	900 000 619	FDA UDI	Class II	Unknown
"Mini Muc"	0489	FDA UDI	Class II	Active
Disposable Respiratory Circuits	9686	FDA UDI	Class II	Active
MADA Aerosol Mask Kits	50311	FDA UDI	Class II	Active
VixOne	0255	FDA UDI	Class II	Unknown
Oxygen Tubing	0005	FDA UDI	Class I	Unknown
Hyperinflation	7-N7905-MAN	FDA UDI	Class II	Active
Pediatric Tracheostomy Mask	0361	FDA UDI	Class I	Active
Disposable anesthesia circuits	9589	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	5705	FDA UDI	Class I	Active
UnoMist™ Nebulizer Mask Kit	3777-E	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	9010	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	9623	FDA UDI	Class I	Active
Heart® Direct Connect Continuous Nebulizer, Adult Kit W/Syringe	100659	FDA UDI	Class II	Unknown
BlockAide Pulmonary Function Filter	6906-6R	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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.