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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 16 of 26

Device	Model / Reference	Registries	Class	Status
Disposable Respiratory Circuits	CA3132	FDA UDI	Class I	Unknown
Comfort Soft Plus CO2 Sampling Nasal Cannula	0587	FDA UDI	Class I	Active
Transpot Kit with Oxygen Mask	9440	FDA UDI	Class II	Active
VixOne Nebulizer	0357	FDA UDI	Class II	Active
Strapette	CP-4204	FDA UDI	Class I	Active
Adult Soft Tip Cannula with 7' 85 Shore Green Tubing	0556	FDA UDI	Class I	Active
MR Patient Care Pediatric LoFlo CO2/O2 Cannulas (20)	P183281	FDA UDI	Class II	Active
Oxygen Tubing	1002280	FDA UDI	Class I	Active
Uni-Lim 72" Adult Coaxail Breathing Circuit	9298	FDA UDI	Class II	Active
Gas Sampling Line	0522	FDA UDI	Class I	Active
Pedi-Neb Nasal Nebulizer	0383	FDA UDI	Class II	Active
Disposable anesthesia circuits	9359	FDA UDI	Class I	Active
Pedi-Lim Breathing Circuit	9023	FDA UDI	Class I	Active
Hme	6388	FDA UDI	Class II	Unknown
Pulset	3103	FDA UDI	Class I	Active
Disposable Respiratory Circuits	MC02810543	FDA UDI	Class I	Active
144"Adult Circuit, Bi-Wye	9579	FDA UDI	Class II	Active
Pulset	3103-91	FDA UDI	Class I	Active
Oxygen Tubing	1002278	FDA UDI	Class I	Active
Pediatric Elongated Venturi Mask Kit	3227-E	FDA UDI	Class I	Active
Disposable Anesthesia Breathing Circuit	8576	FDA UDI	Class I	Active
Pulset	3373-91	FDA UDI	Class I	Active
60" Adult Anesthesia Circuit	9164	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	8234	FDA UDI	Class II	Active
Circulaire II Aerosol Drug Delivery System	0295	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuit	9376	FDA UDI	Class II	Active
Hyperinflation AMBU	900 000 618	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	7-8901-10-62-69	FDA UDI	Class I	Active
BagEasy	562082	FDA UDI	Class II	Unknown
Non-Rebreather Mask	0365	FDA UDI	Class I	Active
NeoPad "T" Power Supply Cable	9400R	FDA UDI	Class II	Active
Water Trap	0221	FDA UDI	Class II	Active
Anesthesia/Breathing Circuits	9396	FDA UDI	Class II	Active
72' Adult Uni-Lim™ Coaxial Anesthesia Circuit	9128	FDA UDI	Class II	Active
60" Expandable Breathing Circuit	9144	FDA UDI	Class I	Active
Berman Oral Airway	7-2091	FDA UDI	Class I	Unknown
Disposable Anesthesia Circuit	8165	FDA UDI	Class I	Active
Gas Sampling Line	0527	FDA UDI	Class I	Unknown
Comfort Soft Plus	0380	FDA UDI	Class I	Active
Anesthesia Circuit, Adult	6717	FDA UDI	Class II	Active
Adult 72" Expandable Circuit	9370	FDA UDI	Class I	Unknown
Gas Sampling Line with Reflective Luer	0941	FDA UDI	Class II	Unknown
Filter	6145	FDA UDI	Class II	Active
Comfort Soft Plus™ FloEasy	0901	FDA UDI	Class I	Unknown
NeoPod	9403	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuit	6794	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	9279	FDA UDI	Class II	Active
BagEasy	562234	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	9357	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9337	FDA UDI	Class I	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.