Is this your brand? Sign in to claim ownership.

WESTMED, INC.

Last updated September 17, 2026

What WESTMED, INC. makes

WestMed, Inc. manufactures single-use and reusable respiratory and anaesthesia devices, including breathing circuits for anaesthesia and ventilators, heat/moisture exchangers, nasal oxygen cannulas (with and without CO₂ sampling), nebulizing delivery sets, arterial blood sampling kits, and oxygen administration tubing. Their portfolio also covers infant resuscitation circuits and aerosol drug delivery systems.

The company’s products are regulated under FDA’s Class I and Class II device classifications and are listed in the FDA’s Unique Device Identifier (UDI) database. WestMed, Inc. is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

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 21 of 26

Device	Model / Reference	Registries	Class	Status
Anesthesia Circuit	9691	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	7-8103	FDA UDI	Class I	Unknown
96" Adult Anesthesia Circuit	9261	FDA UDI	Class I	Active
Aerosol Masks	0300	FDA UDI	Class I	Active
Anesthesia Circuit Kit	R-9045	FDA UDI	Class II	Active
Heart® Direct Connect Cont.Nebulizer, Ped. SuperSpike, 3cc Sy	100627	FDA UDI	Class II	Unknown
Adult Nasal Cannula for GI Source	08-0006	FDA UDI	Class I	Active
BagEasy	562233	FDA UDI	Class II	Unknown
Disposable Circuit	8303	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	9292	FDA UDI	Class II	Active
Anapod Breathing Circuit	A9243	FDA UDI	Class II	Unknown
Comfort Soft Plus™ Cannula FloEasy	0902	FDA UDI	Class I	Unknown
Adult, Dual Limb Circuit	8225	FDA UDI	Class II	Unknown
Adapters/Connectors	7-5108	FDA UDI	Class I	Active
Device Respiratory Accessory Kit	0791	FDA UDI	Class I	Active
Pulset	3312-91	FDA UDI	Class I	Active
Uni-Lim 72" Adult Coaxail Breathing Circuit	9177	FDA UDI	Class II	Active
Berman Oral Airway	7-2101	FDA UDI	Class I	Unknown
Anesthesia Circuit Kit	9665	FDA UDI	Class I	Active
Vibralung Patient Kit with Circulair II Model 0295	9605-10	FDA UDI	Class II	Active
Circulaire II Aerosol Drug Delivery System	0395	FDA UDI	Class II	Active
Comfort Soft Plus™ Cannula	0810	FDA UDI	Class I	Active
Oxygen Tubing, KROT, 14' (S)	0014	FDA UDI	Class I	Active
Disposable, Non-Heated Adult Passive Circuit	6564	FDA UDI	Class II	Active
FloEasy	9570HTS	FDA UDI	Class II	Unknown
Comfort Soft Plus	0197-RC	FDA UDI	Class I	Active
Nebulizers	1002223	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	7-9200	FDA UDI	Class I	Active
Disposable Anesthesia Circuit	9611	FDA UDI	Class I	Unknown
Nebulizers	1002221	FDA UDI	Class II	Active
Flex Extenders	7-5132	FDA UDI	Class I	Active
Gas Sampling Line	0533	FDA UDI	Class I	Active
Anesthesia Circuit Kit	9809	FDA UDI	Class I	Active
Disposable Respiratory Circuits	9288	FDA UDI	Class I	Active
Anapod™ Humi-therm Heated and Humidified Wick Breathing Circuit	A9244	FDA UDI	Class II	Unknown
Anapod™ Humi-therm Heated and Humidified Wick Breathing Circuit	A9241	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	8012	FDA UDI	Class I	Active
Berman Oral Airway	1002263	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	7-8901-10-62	FDA UDI	Class I	Active
Bubble Humidifier	010-104858	FDA UDI	Class I	Active
Mask, Adult, Non-Rebreather, W/Safety Vent, 7' KROT	1326	FDA UDI	Class I	Active
Anesthesia Circuit Kit	R-9046	FDA UDI	Class II	Active
Cannula, Adult High Flow	0551	FDA UDI	Class I	Active
Gas Sampling Line	0802	FDA UDI	Class II	Unknown
Circulaire II Hybrid Aerosol Drug Delivery System	0396	FDA UDI	Class II	Active
MR Patient Care Adult LoFlo CO2 with O2 Cannulas (20)	P183271	FDA UDI	Class II	Active
Breathing Bag	S6569P	FDA UDI	Class I	Active
BagEasy	562136	FDA UDI	Class II	Unknown
Hyperinflation	7-N7905-N	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	6790	FDA UDI	Class II	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.

Westmed, Inc. has 26 recall records initiated between June 22, 2010, and September 27, 2024, with statuses recorded as open, classified, or terminated. The reasons cited include manufacturing inconsistencies in adapter dimensions affecting compatibility with infant resuscitators, potential loose connections in oxygen delivery systems, non-specified connector failures in circuit flex extenders, a supplier recall involving alcohol pads, and a reported disconnection risk at the patient port retention ring assembly of a manual resuscitation device.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

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.