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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 2 of 26

Device	Model / Reference	Registries	Class	Status
72" Pediatric Anesthiesa Breathing Circuit	9180	FDA UDI	Class I	Active
Vibralung®	9641	FDA UDI	Class II	Active
Disposable Anesthesia Circuit	9393	FDA UDI	Class I	Unknown
BagEasy	562202	FDA UDI	Class II	Active
Disposable Anesthesia Breathing Circuit	9668	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9008	FDA UDI	Class II	Unknown
Comfort Soft Plus®	R-0556-5-20	FDA UDI	Class I	Active
BagEasy	562203	FDA UDI	Class II	Unknown
Anesthesia/Breathing Circuits	9702	FDA UDI	Class II	Unknown
Patient Protection Mask	PPM-Kit	FDA UDI	Class II	Active
Adaptors/Connectors	S6262	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	8273N	FDA UDI	Class II	Unknown
Pedi-Lim Breathing Circuit	9024	FDA UDI	Class I	Active
Filter	6218	FDA UDI	Class II	Active
MicroBlock	CMI-2716E	FDA UDI	Class II	Active
Chinstrap	CP-5100	FDA UDI	Class I	Unknown
Hyperinflation (AMBU)	900 000 604	FDA UDI	Class II	Active
96" Adult Expandable Circuit, swivel Wye, Large Mask	9653	FDA UDI	Class II	Unknown
Comfort Soft Plus	0562-02	FDA UDI	Class II	Active
Muc-Away, Comfort Soft	0491	FDA UDI	Class II	Active
Pulset	3700	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	6883	FDA UDI	Class II	Active
High Flow Transport Circuit	9405	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	7-8900	FDA UDI	Class I	Active
Pro-Nox	PROMEDKIT	FDA UDI	Class I	Active
60" Adult Anesthesia Circuit	9211	FDA UDI	Class I	Active
Circulaire II Aerosol Drug Delivery System	0329	FDA UDI	Class II	Active
Mask	1002224	FDA UDI	Class I	Active
Blood Gas Sampler	3105-95VT	FDA UDI	Class I	Unknown
Bracket with Tube Guide	WP-7704	FDA UDI	Class II	Active
Bubble Humidifier	1002248	FDA UDI	Class I	Active
Adult 108" Expandable Breathing Circuit	9157	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	9316	FDA UDI	Class I	Active
VixOne	0210-14	FDA UDI	Class II	Active
Heart® Direct Connect Continuous Nebulizer	100610	FDA UDI	Class II	Active
Mini-HEART®	100612	FDA UDI	Class II	Active
Anesthesia Circuit Kit	9805	FDA UDI	Class I	Active
Hyperinflation	7-N7903-62	FDA UDI	Class II	Active
Composite Kit	0794	FDA UDI	Class II	Unknown
Bacterial/Viral Filter	010-105474	FDA UDI	Class II	Active
Disposable Respiratory Circuits	8121	FDA UDI	Class II	Active
Breathing Bag	7-6201	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuit	9003	FDA UDI	Class I	Active
SavEar	RT-6100	FDA UDI	Class I	Active
VixOne Nebulizer	0240	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	9033	FDA UDI	Class I	Active
Double Limb Circuit	9683	FDA UDI	Class I	Unknown
Anesthesia Mask	7-9902	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	9574	FDA UDI	Class I	Active
Anesthesia Circuit Kit	R-6619	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

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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.