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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 5 of 26

Device	Model / Reference	Registries	Class	Status
144" Pediatric Anesthesia Circuit	9204	FDA UDI	Class I	Active
Anesthesia Circuit Kit	R-7-8600	FDA UDI	Class II	Active
Adult Nasal Cannula for GI Source	08-0008	FDA UDI	Class I	Active
O2 Composite Kit	HCO100	FDA UDI	Class II	Active
Comfort Soft Plus, Infant	0173	FDA UDI	Class I	Active
VixOne™ Nebulizer Mask Kit	0362	FDA UDI	Class II	Active
Ventilator Connecting Hose	5081-Rev_D	FDA UDI	Class I	Active
Adult CO2/ O2 Mask	0930	FDA UDI	Class II	Active
Uni-Lim, 60" Adult Coaxial Circuit	6653	FDA UDI	Class II	Active
BlockAide Pulmonary Function Filter	6903-3E	FDA UDI	Class II	Active
Hyperinflation	MC79020220	FDA UDI	Class II	Active
Neo-Vent™	0419	FDA UDI	Class II	Unknown
Comfort Soft Plus CO2 Sampling Nasal Cannula	0503-01	FDA UDI	Class II	Unknown
CO2/O2 Nasal Cannula	0912	FDA UDI	Class II	Unknown
O2 Kit: Peoples Medical	0875	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	8079	FDA UDI	Class II	Active
Anesthesia Circuits	9057	FDA UDI	Class I	Active
Pulset	3303-50	FDA UDI	Class II	Active
Hmef	010-105564	FDA UDI	Class I	Active
Pulset	3105+	FDA UDI	Class II	Active
Sensor Wrap	CP-0005	FDA UDI	Class I	Unknown
CO2 Sampling Nasal Cannula	0502	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	8100	FDA UDI	Class II	Active
72`Adult Uni-Lim™, GSE 2 BV Filter 3L	9269	FDA UDI	Class II	Active
Comfort Soft Plus	1002345	FDA UDI	Class I	Active
Anesthesia/Breathing Circuits	9699	FDA UDI	Class II	Unknown
MR Patient Care LoFlo CO2 with Airway Adapters (20)	P183291	FDA UDI	Class I	Active
Comfort Soft Plus™ Adult High Flow Cannula	0547	FDA UDI	Class I	Unknown
Neo-Vent Infant T-Piece Resuscitation Circuit	0415	FDA UDI	Class II	Unknown
Hyperinflation	900 000 627	FDA UDI	Class II	Unknown
96" Adult Anesthesia Circuit	9175	FDA UDI	Class II	Active
MADA Up-Mist Medication Nebulizer	1312	FDA UDI	Class II	Active
Comfort Soft Plus, Infant Nasal Cannula	0858	FDA UDI	Class I	Active
Heart® Continuous Nebulizer Holder	100950	FDA UDI	Class II	Unknown
60" Pediatric Anesthesia Circuit	9162	FDA UDI	Class I	Active
Berman Oral Airway	7-2071	FDA UDI	Class II	Unknown
Uni-Lim, 72" Adult Coaxial Circuit	8580	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	CA3106	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	8139	FDA UDI	Class I	Active
Disposable Anesthesia Breathing Circuit	5705-S	FDA UDI	Class I	Active
Micro Cannula	0137	FDA UDI	Class I	Active
Nebulizer	0200	FDA UDI	Class II	Active
MicroBlock	CMI-2714E	FDA UDI	Class II	Active
A-Line 3cc Syringe	3300-30	FDA UDI	Class I	Active
Adaptors/Connectors	S6230	FDA UDI	Class I	Unknown
Pulset	3363-91	FDA UDI	Class I	Active
Pulset	3363-95S	FDA UDI	Class I	Active
Disposable Anesthesia Circuit	7-9529	FDA UDI	Class I	Unknown
Adaptor	0238	FDA UDI	Class II	Unknown
Filter	6396	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

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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.