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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 18 of 26

Device	Model / Reference	Registries	Class	Status
Hyperinflation	7-N7901-MAN	FDA UDI	Class II	Active
Uni-Heart™ Lo-Flo Continuous Nebulizer	100850	FDA UDI	Class II	Active
Disposable anesthesia circuits, Adult 96"	8973	FDA UDI	Class II	Unknown
Mini-Heart® Continuous Nebulizer	100611	FDA UDI	Class II	Active
Berman Oral Airway	7-2081	FDA UDI	Class I	Unknown
BagEasy	562081	FDA UDI	Class II	Unknown
Uni-Lim 120" Adult Coaxial Breathing Circuit	9096	FDA UDI	Class II	Active
WaterPAP Pro	WP-7800	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	8833	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	8005	FDA UDI	Class II	Unknown
Tracheostomy Masks	0360	FDA UDI	Class I	Active
Pulset	3105-95	FDA UDI	Class I	Unknown
Adult Face Tent	0356	FDA UDI	Class I	Unknown
Heart®Direct Connect, Continuous Nebulizer, Pediatric Kit	100629	FDA UDI	Class II	Active
AMBU Co2 Detector	000-172-712	FDA UDI	Class II	Active
72"Adult Circuit, Bi-Wye	9567	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	6719	FDA UDI	Class I	Unknown
Pulset	3353-95	FDA UDI	Class I	Active
VixOne	0225	FDA UDI	Class II	Unknown
Pulset	3302-95+	FDA UDI	Class II	Active
108" Pediatric Anesthesia Circuit	9159	FDA UDI	Class I	Active
WaterPAP™ Starter Kit	WP-7705	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	7-9211-10	FDA UDI	Class II	Unknown
Mini-Heart	100625	FDA UDI	Class II	Active
Pressure Safe™ CSP	0885	FDA UDI	Class I	Active
Pulset	3342-95	FDA UDI	Class I	Active
Filter	6370	FDA UDI	Class II	Active
Disposable Respiratory Circuits	9424	FDA UDI	Class II	Active
Aerosol Tee	0219	FDA UDI	Class I	Unknown
Pulset	3300-95	FDA UDI	Class I	Active
Pulset	3173-95	FDA UDI	Class I	Unknown
Anesthesia Circuit Kit	R-9337	FDA UDI	Class II	Active
OxyGo Adult Cannula	1425-1002	FDA UDI	Class I	Active
Berman Oral Airway	7-2041	FDA UDI	Class I	Unknown
Transport Circuit	8073	FDA UDI	Class II	Unknown
Ambu Hyper System	900 000 616	FDA UDI	Class II	Unknown
Disposable Circuit	8306	FDA UDI	Class II	Unknown
Vented Luer Tip Cap	0405	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	8264	FDA UDI	Class I	Unknown
Pro-N20	9303	FDA UDI	Class II	Active
Pulset	3173-14	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	7-8113-10-62-68	FDA UDI	Class II	Active
Uni-Lim 40" Coaxial Circuit	6656	FDA UDI	Class I	Active
Disposable Anesthesia Circuit	9599	FDA UDI	Class II	Active
Gas Sampling Line	0514	FDA UDI	Class I	Active
MicroBlock	CMI-2713E	FDA UDI	Class II	Active
Hyperinflation AMBU	900 000 625	FDA UDI	Class II	Unknown
Pedi-lim 72" Pediatric Coaxial Anesthesia Circuit	9627	FDA UDI	Class I	Unknown
Atellica® VTR Syringes	11561349	FDA UDI	Class II	Active
Uni-Lim 60" Anesthesia Breathing Circuit	9091	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

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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.