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 23 of 26

Device	Model / Reference	Registries	Class	Status
Berman Oral Airway	7-2061	FDA UDI	Class I	Unknown
Anesthesia Mask	7-9910	FDA UDI	Class I	Active
Circulaire Aerosol Drug Delivery System	0394	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	8026	FDA UDI	Class I	Unknown
Disposable Hyperinflation System	7-N7905-I-MAN-P	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	8695	FDA UDI	Class II	Unknown
Blood Gas Sampler	ABG-3601-VS	FDA UDI	Class I	Active
Disposable Heated Humidified Circuit Kit	9655	FDA UDI	Class II	Active
Corrugated Hose	0465	FDA UDI	Class I	Active
Neo-Vent™, Humidified Infant T-Piece Resuscitation Kit	0422	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	7-7202-66	FDA UDI	Class I	Unknown
Comfort Soft Plus CO2 Sampling Nasal Cannula	0581	FDA UDI	Class I	Active
Nebulizer	0319	FDA UDI	Class II	Active
Uni-Lim 84" Adult Coaxial Circuit	8057	FDA UDI	Class II	Active
OxyGo Oxygen Tubing	1425-1009	FDA UDI	Class I	Active
TubeCatch	TC-1022	FDA UDI	Class I	Active
Disposable anesthesia circuits	9045	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	7-8113-10-62	FDA UDI	Class II	Active
Comfort Soft Plus™ Adult Nasal Cannula w/25' KROT Tubing, Green	0589	FDA UDI	Class I	Active
Nebulizers	1002342	FDA UDI	Class II	Active
WaterPAP™ Pro Starter Kit	WP-7805	FDA UDI	Class II	Unknown
Cannula, Adult, Soft Tip, w/50' KROT	0196	FDA UDI	Class I	Active
Comfort Soft Plus	1002275	FDA UDI	Class I	Active
Tube Tackles	CP-0400	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	8229	FDA UDI	Class II	Active
Pulset	3105-91	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	7-7201-66	FDA UDI	Class I	Unknown
Nebulizer	0311	FDA UDI	Class II	Active
Mini-Heart® Lo-Flo Continuous Nebulizer	100611B	FDA UDI	Class II	Active
Pedi-Neb Nasal Nebulizer	0384	FDA UDI	Class II	Active
Pulset	3302-95	FDA UDI	Class I	Unknown
Pedi-Lim Co-axial Circuit	9138	FDA UDI	Class I	Active
HyperInflation	7-N7901-62	FDA UDI	Class II	Active
Corrugated Hose	0466	FDA UDI	Class I	Unknown
Comfort Soft Plus	0567-RC	FDA UDI	Class I	Active
Uni-Lim 72" Adult Coaxail Breathing Circuit	6884	FDA UDI	Class I	Active
Anapod	9240HT	FDA UDI	Class II	Unknown
Comfort Soft Plus®	R-0556-10-10	FDA UDI	Class I	Active
Adult CO2 /O2 Mask	0562F	FDA UDI	Class II	Active
Uni-Lim 120" Adult Coaxial Breathing Circuit	9618	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9148	FDA UDI	Class I	Active
Uni-Lim Coaxail Breathing Circuit	9432	FDA UDI	Class I	Active
Heated circuit	9411	FDA UDI	Class II	Unknown
Hepa Filter	1002217	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	51260A-5686	FDA UDI	Class II	Active
Oxygen Tubing	1002281	FDA UDI	Class I	Active
Hyperinflation (AMBU)	900 000 602	FDA UDI	Class II	Active
Disposable anesthesia circuits	9593	FDA UDI	Class I	Active
Pulset™ 1cc Syringe	3105 MX	FDA UDI	Class I	Unknown
Anesthesia Circuit	9670	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.