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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 9 of 26

Device	Model / Reference	Registries	Class	Status
Pulset	3393	FDA UDI	Class I	Unknown
CO2 Sampling Nasal Cannula	0541	FDA UDI	Class II	Active
Comfort Soft Plus CO2 Sampling Nasal Cannula	0441F	FDA UDI	Class I	Active
Nebulizer	0312	FDA UDI	Class II	Active
Neo-Vent Infant T-Piece Resuscitation Circuit w/Infant Mask	0420	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	61272A	FDA UDI	Class II	Active
HEPA Filter	F300A	FDA UDI	Class II	Unknown
VixOne	0222	FDA UDI	Class II	Active
Uni-Lim Coaxial Circuit	9697	FDA UDI	Class II	Unknown
Adapters/Connectors	7-5119	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	AC7000	FDA UDI	Class II	Unknown
Mask	1002219	FDA UDI	Class I	Active
Breathing Bag	7-6206	FDA UDI	Class I	Active
Mouthpiece, Smooth 22mm	0429	FDA UDI	Class I	Unknown
Anesthesia/Breathing Circuits	6901	FDA UDI	Class I	Active
Pulset 3cc Syringe Safety Tip	3362-91S	FDA UDI	Class I	Unknown
Adaptors/Connectors	S6232	FDA UDI	Class I	Unknown
Anapod Transport Circuit	9411	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	8090	FDA UDI	Class I	Active
CSP, Premature Nasal Cannula	0883	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	6015	FDA UDI	Class I	Unknown
Disposable anesthesia circuits	9358	FDA UDI	Class I	Active
60" Uni-Lim Adult Anesthesia Circuit	9617	FDA UDI	Class II	Active
BagEasy® Resuscitator	R-562080	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuit	9673	FDA UDI	Class II	Active
72" Anesthesia Breathing Circuit	9228	FDA UDI	Class I	Active
Adult Oral/Nasal Cannula	0911	FDA UDI	Class II	Unknown
Anesthesia Mask	7-9530	FDA UDI	Class I	Unknown
Anesthesia Mask	7-9911	FDA UDI	Class I	Unknown
Circulaire Aerosol Drug Delivery System	0272	FDA UDI	Class II	Unknown
Filter	6216	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	8065	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	CP3113	FDA UDI	Class II	Unknown
Transport Kit with Adult Elongated Non-Rebreather Mask with Safety Vent	9442	FDA UDI	Class II	Active
Pulset™ 3CC Syringe, 23G X 1", Safety Tip, 25U BH	3303-91	FDA UDI	Class I	Active
VixOne	0235	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuit	9372	FDA UDI	Class I	Active
Bacterial/Viral Respiratory Filter	0242	FDA UDI	Class II	Unknown
Aerosol Masks	0251	FDA UDI	Class I	Active
Capette	CP-4202	FDA UDI	Class I	Active
Comfort Soft Plus	0441	FDA UDI	Class I	Active
VixOne	0294	FDA UDI	Class II	Unknown
Hyperinflation	7-N7905-62	FDA UDI	Class II	Active
Gas Sampling Line	0520	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	8025	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	7-7205-66	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	9046	FDA UDI	Class I	Active
Anesthesia Masks	7-7700	FDA UDI	Class I	Unknown
Cannula, Adult, Soft Tip, W/7' KROT, EarMates WO/Slit	0553	FDA UDI	Class I	Active
Disposable Anesthesia Circuit	8259	FDA UDI	Class I	Unknown

Related Companies

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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.