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 19 of 26

Device	Model / Reference	Registries	Class	Status
Mini-Heart ® Lo-Flo Continuous Nebulizer	100611A	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	7-8303-10	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	9278	FDA UDI	Class I	Active
Comfort Soft Plus, Premature Soft-Tipped Cannula	0157	FDA UDI	Class I	Unknown
BagEasy	562048	FDA UDI	Class II	Unknown
BagEasy	562190	FDA UDI	Class II	Unknown
VixOne	0210	FDA UDI	Class II	Active
BagEasy	562084	FDA UDI	Class II	Unknown
Adaptors/Connectors	0487	FDA UDI	Class I	Unknown
Gas Sampling Line	0510	FDA UDI	Class I	Unknown
OxyGo Inline Water Trap, For Oxygen Delivery	1425-1013	FDA UDI	Class II	Active
Filter	A38605HP	FDA UDI	Class II	Unknown
Uni-lim Coaxial Circuit	9415	FDA UDI	Class I	Active
Variable Pressure Safe™ Large Infant Nasal Cannula	0880	FDA UDI	Class I	Unknown
Pulset Arterial Blood Gas Syringe	3393CH	FDA UDI	Class I	Unknown
A-Line	3100-28	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	6844	FDA UDI	Class I	Active
Comfort Soft Plus	1002162	FDA UDI	Class I	Active
Tubing	2188	FDA UDI	Class I	Active
Comfort Soft Plus™ FloEasy	0900	FDA UDI	Class I	Unknown
Nebulizer	0313	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	6789	FDA UDI	Class II	Unknown
Chinstrap	CP-5200	FDA UDI	Class I	Unknown
Comfort Soft Plus, Premature Nasal Cannula	0857	FDA UDI	Class I	Active
Heart®Direct Connect, Continuous Nebulizer, Pediatric Kit	100639	FDA UDI	Class II	Active
Guedel Airways	7-3551	FDA UDI	Class I	Unknown
MR Patient Care Pediatric LoFlo CO2/O2 Cannulas (100)	P185371	FDA UDI	Class II	Active
Nebulizer	0310	FDA UDI	Class II	Active
VixOne Nebulizer	0233	FDA UDI	Class II	Active
Pulset	3362-95	FDA UDI	Class I	Unknown
MADA Aerosol Mask Kits	50310	FDA UDI	Class II	Unknown
Cannula, Adult High Flow	0549	FDA UDI	Class I	Unknown
Disposable Respiratory Circuits	7-9022	FDA UDI	Class I	Active
FeedSafe	0851	FDA UDI	Class I	Active
Anesthesia Circuit Kit	9812	FDA UDI	Class I	Active
OxyGo Comfort Soft Plus® Adult Cannula	1425-1004	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	8039	FDA UDI	Class II	Active
Atellica® VTR Syringes	11561352	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9340	FDA UDI	Class II	Active
Pro-N2O	WES-PROAESKIT	FDA UDI	Class I	Active
Adult Nasal Cannula, Soft Tip, 14' Tubing, W/Threaded Nut	0568	FDA UDI	Class I	Active
Comfort Soft Plus	010-0050	FDA UDI	Class I	Active
Uni-lim Coaxial Circuit	9566	FDA UDI	Class I	Active
Flex Extenders	S6419P	FDA UDI	Class I	Active
Berman Oral Airway	7-2051	FDA UDI	Class I	Unknown
Hyperinflation	7-N7902-62	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9007	FDA UDI	Class II	Unknown
BlockAide Pulmonary Function Filter	6904-4R	FDA UDI	Class II	Active
50' Oxygen Tubing, Green, Bulk	0052B	FDA UDI	Class I	Active
Adult Nasal Cannula, Soft Tip, 7' Tubing W/Threaded Nut	0567	FDA UDI	Class I	Unknown

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.