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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 22 of 26

Device	Model / Reference	Registries	Class	Status
Uni-Lim Circuit	9170	FDA UDI	Class I	Active
Atellica® VTR Syringes	11561342	FDA UDI	Class II	Active
A-Line	3332-91	FDA UDI	Class I	Active
Cannula	5312	FDA UDI	Class I	Unknown
Corrugated Tubing Cuttable Cuffs	1002060	FDA UDI	Class I	Active
Nose Clip	0404	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	7-SP5624	FDA UDI	Class II	Active
Comfort Soft Plus	0568-RC	FDA UDI	Class I	Active
BlockAide Pulmonary Function Filter	6903-3R	FDA UDI	Class II	Active
A-Line	3300-26	FDA UDI	Class I	Active
Strapette	CP-4404	FDA UDI	Class I	Active
Oxygen Tubing 50' Bulk	0050B	FDA UDI	Class I	Active
Dual--Lumen Cannula	10035469	FDA UDI	Class I	Active
Disposable Anesthesia Breathing Circuit	9110	FDA UDI	Class I	Active
Comfort Soft Plus, Adult	0536	FDA UDI	Class I	Unknown
Anesthesia Circuit Kit	R-9003	FDA UDI	Class II	Active
Circulaire Aerosol Drug Delivery System	0321	FDA UDI	Class II	Unknown
Mini-HEART®	100612A	FDA UDI	Class II	Active
HEPA Filter	6234	FDA UDI	Class II	Active
Adaptors/Connectors	S1137	FDA UDI	Class I	Active
Capette	CP-4201	FDA UDI	Class I	Active
Anapod Humi-Therm	9240HTS	FDA UDI	Class II	Unknown
BagEasy	562237	FDA UDI	Class II	Unknown
Pulset	3303-95S	FDA UDI	Class I	Active
MR Patient Care Neonatal LoFlo CO2 with Cannulas (20)	P183261	FDA UDI	Class II	Active
A-Line	3300-24BC	FDA UDI	Class I	Unknown
Tubing	9687	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuits	7-8113-10-36-56	FDA UDI	Class II	Active
Hmef	1002261	FDA UDI	Class I	Active
Anesthesia Circuit Kit	R-8856	FDA UDI	Class II	Active
Disposable Anesthesia Circuit	9325	FDA UDI	Class II	Active
Capette	CP-4401	FDA UDI	Class I	Active
Nebulizer	0309	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9002	FDA UDI	Class II	Active
Barbed Oxygen Connector	0043	FDA UDI	Class I	Active
Gas Sampling Line	0519	FDA UDI	Class I	Unknown
Berman Airways	7-0090	FDA UDI	Class I	Unknown
Guedel Airways	7-3601	FDA UDI	Class I	Unknown
Adult Face Tent	111-E	FDA UDI	Class I	Active
Uni-Lim™ Adult Elbow	9565	FDA UDI	Class II	Active
Disposable Medical Hyperinflation System	0426	FDA UDI	Class II	Active
CO2 Sampling Nasal Cannula	B180030C	FDA UDI	Class I	Active
Pulset	3300	FDA UDI	Class I	Active
Cannula, Adult, Soft Tip w/2` Connector	0190	FDA UDI	Class I	Unknown
Bubble Humidifier	1002283	FDA UDI	Class I	Active
Composite Respiratory Kit	0797	FDA UDI	Class I	Active
Non-Rebreather Mask	0367	FDA UDI	Class I	Unknown
Capette	CP-4402	FDA UDI	Class I	Active
Anesthesia Circuit Kit	R-6844	FDA UDI	Class II	Active
UniHeart™ Lo-Flo Continuous Nebulizer, Ped.Super Spike Mask	100942	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

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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.