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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 20 of 26

Device	Model / Reference	Registries	Class	Status
Variable Pressure Safe™ Neonate Nasal Cannula	0878	FDA UDI	Class I	Unknown
Valve, Bleed Tail	7-00675	FDA UDI	Class II	Active
Cannula, Adult Nasal, Soft Tip, W/7' KROT	0197	FDA UDI	Class I	Unknown
IV-Heart™ Continuous Nebulizer Pediatric Kit	101022	FDA UDI	Class II	Active
Anesthesia Circuit	9669	FDA UDI	Class II	Active
Barbed Tubing Adaptor	0409	FDA UDI	Class I	Active
Filter	7-SP5125	FDA UDI	Class II	Unknown
Adapter, 22mm X 6mm	CP-2209	FDA UDI	Class I	Active
Anesthesia Circuit	9363	FDA UDI	Class II	Active
Comfort Soft Plus	1002347	FDA UDI	Class I	Active
Cannula	2100-W	FDA UDI	Class II	Active
Anesthesia Mask	6387	FDA UDI	Class I	Unknown
BlockAide Pulmonary Function Filter	6905-5R	FDA UDI	Class II	Active
Anesthesia Circuit Kit	R-9303	FDA UDI	Class II	Active
NeoPod T	4007-1	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	7350	FDA UDI	Class I	Unknown
Anesthesia Circuit Kit	R-8156	FDA UDI	Class II	Active
Pulset	3363-95	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	9273	FDA UDI	Class I	Active
Filter	6158	FDA UDI	Class II	Unknown
Pulset™	3165-91	FDA UDI	Class I	Active
Guedel Airway	7-3571	FDA UDI	Class I	Unknown
Anesthesia Circuit Kit	R-7-9201-10-62	FDA UDI	Class II	Active
120" Anesthesia Breathing Circuit	9187	FDA UDI	Class II	Active
Aerosol Masks	260-E	FDA UDI	Class I	Active
Hygrobac `S` Filter, W/Elbow	MC58770254	FDA UDI	Class II	Unknown
Anesthesia Mask	7-SP5613	FDA UDI	Class I	Unknown
BlockAide Pulmonary Function Filter	6906-6E	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	7-8911-10	FDA UDI	Class II	Active
Disposable Anesthesia Circuit	9674	FDA UDI	Class I	Active
Jackson Rees Anesthesia Circuit	6135	FDA UDI	Class I	Unknown
CO2/O2 Oral/Nasal Cannula	0917	FDA UDI	Class II	Unknown
120" Adult Anesthesia Circuit	9227	FDA UDI	Class II	Active
Adult Anesthesia Expandable Circuit	9590	FDA UDI	Class I	Active
FeedSafe	0850	FDA UDI	Class I	Active
Comfort Soft Plus Adult Cannula High Flow	0550-TN	FDA UDI	Class I	Unknown
CSP, Neonatal Nasal Cannula	0884	FDA UDI	Class I	Unknown
Comfort Soft Plus CO2 Sampling Nasal Cannula	0860	FDA UDI	Class I	Unknown
Septal-H	CP-5400	FDA UDI	Class I	Active
Adapters/Connectors	7-5114	FDA UDI	Class I	Active
BagEasy	562048DM	FDA UDI	Class II	Unknown
Anesthesia Circuit Kit	R-9422	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	6723	FDA UDI	Class I	Active
Nebulizer	0223	FDA UDI	Class II	Active
A-Line	3333-91	FDA UDI	Class I	Active
Hyperinflation (AMBU)	900 000 610	FDA UDI	Class II	Unknown
VixOne	0218	FDA UDI	Class II	Active
Vibralung Trach Interface Kit with Aerosol Delivery System	9646	FDA UDI	Class II	Active
Adaptors/Connectors	7-5126	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	8632	FDA UDI	Class II	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.