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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 24 of 26

Device	Model / Reference	Registries	Class	Status
Pediatric Soft Tip Cannula	0183	FDA UDI	Class I	Unknown
Face Mask, Pediatric	7-9803	FDA UDI	Class I	Unknown
*Mini-Heart® Lo-Flo, Continuous Nebulizer, Adult Valve Tee	100623	FDA UDI	Class II	Active
Anesthesia/Breathing Circuits	9395	FDA UDI	Class I	Active
Pulset	3344-95	FDA UDI	Class I	Active
Uni-Lim 72" Adult Coaxail Breathing Circuit	9161	FDA UDI	Class II	Active
FloEasy Co-Flo, Disposable Heated Humidified Circuit Kit	9571	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	7-8300	FDA UDI	Class I	Unknown
Anesthesia Circuit Kit	9808	FDA UDI	Class I	Active
VixOne	0229	FDA UDI	Class II	Active
72: Adult Respiratory Circuit	9289	FDA UDI	Class I	Unknown
BagEasy	562013	FDA UDI	Class II	Unknown
Adult Expandable Circuit	9698	FDA UDI	Class II	Unknown
Earmates	0440	FDA UDI	Class II	Unknown
Hyperinflation (AMBU)	900 000 606	FDA UDI	Class II	Active
Tube Tackles	CP-0200	FDA UDI	Class I	Active
Composite Respiratory Kit: Performance Home Medical	0836	FDA UDI	Class II	Active
Pulset	3302-95S	FDA UDI	Class I	Active
Uni-Lim 120" Adult Coaxial Breathing Circuit	6882	FDA UDI	Class I	Active
Disposable Anesthesia Circuit	9598	FDA UDI	Class I	Active
NeoPad "T" AC to DC Power Supply Cable	9401	FDA UDI	Class II	Unknown
Vibralung Patient Kit	9600	FDA UDI	Class II	Active
Disposable Anesthesia Circuit	9597	FDA UDI	Class II	Unknown
Oxygen Tubing, 40' KROT, Green	0042	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	8244	FDA UDI	Class II	Active
Pressure Safe™ CSP	0882	FDA UDI	Class I	Active
Disposable Respiratory Circuits	7-9019	FDA UDI	Class I	Active
Hyperinflation	7-N7905-MAN-P	FDA UDI	Class II	Active
Anesthesia Mask	7-SP5591	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	51260A-5685	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9050	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	8626	FDA UDI	Class I	Active
Pulmonary Hygiene Kit	0393R-10	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	8156	FDA UDI	Class I	Active
Mini-Heart ®Hi-Flo Continuous Nebulizer, Swivel Adaptor	100615	FDA UDI	Class II	Unknown
Comfort Soft Plus, Neonatal Soft-Tip Cannula	0167	FDA UDI	Class I	Active
FloEasy Co-Flo, Disposable Heated Humidified Circuit Kit	9572	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuit	8857	FDA UDI	Class I	Unknown
Anesthesia Mask	7-9905	FDA UDI	Class I	Unknown
Muc-Away	0492	FDA UDI	Class II	Active
Unli-Lim Adult Anesthesia Breathing Circuit	9238	FDA UDI	Class II	Active
Nasal Cannula	0556-EM	FDA UDI	Class I	Active
BlockAide Pulmonary Function Filter	6902-2R	FDA UDI	Class II	Active
Adult Nasal Cannula for GI Source	08-0001	FDA UDI	Class I	Active
Gas Sampling Line	0939	FDA UDI	Class II	Unknown
Gas Sampling Line w/ Tee Adapter	0942	FDA UDI	Class I	Unknown
Mask, Adult Aerosol, Vented	0250	FDA UDI	Class I	Active
Nebulizers	1002350	FDA UDI	Class II	Active
VixOne, Infant	0234	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	8613	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

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Importers

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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.