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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 8 of 26

Device	Model / Reference	Registries	Class	Status
Septal-H	CP-5510	FDA UDI	Class I	Active
Vixone Reusable Nebulizer	0398	FDA UDI	Class II	Active
UnoMist™ Small Volume Nebulizer	3775-E	FDA UDI	Class II	Active
WaterPAP Pole Clamp	CP-2203	FDA UDI	Class II	Active
Disposable Anesthesia Breathing Circuits	8144	FDA UDI	Class I	Unknown
Neo-Pod™ "T"	9403U	FDA UDI	Class II	Unknown
Mask	1002250	FDA UDI	Class I	Active
Mask	1002251	FDA UDI	Class I	Active
Filter	6220	FDA UDI	Class II	Active
Comfort Soft Plus CO2 Sampling Nasal Cannula	0861	FDA UDI	Class I	Active
Hyperinflation (AMBU)	900 000 612	FDA UDI	Class II	Unknown
Comfort Soft Plus	1002235	FDA UDI	Class I	Active
Strapette	CP-4220	FDA UDI	Class I	Active
Disposable Anesthesia Circuits	9335	FDA UDI	Class I	Active
VixOne	0248	FDA UDI	Class II	Unknown
Filter	A4354	FDA UDI	Class II	Unknown
Septal-H	CP-5500	FDA UDI	Class I	Active
*Mini-Heart® Lo-Flo Continuous Nebulizer W/Extension Set, 7'	100616	FDA UDI	Class II	Unknown
96" Pediatric Anesthesia Circuit	9200	FDA UDI	Class I	Active
Adult Nasal Cannula for GI Source	08-0003	FDA UDI	Class I	Active
Cadwell Sleepmate	302543-200-0484	FDA UDI	Class I	Active
Filter	7-00-282	FDA UDI	Class II	Active
Uni-Lim Adult Coaxial Circuit	9190	FDA UDI	Class I	Active
Atellica® VTR Syringes	11561343	FDA UDI	Class II	Active
Pulset	3302	FDA UDI	Class I	Unknown
Nebulizers	1002343	FDA UDI	Class II	Active
MADA Non-Rebreather Masks	53226	FDA UDI	Class I	Active
72" Pediatric Anesthesia Circuit	9223	FDA UDI	Class I	Active
OxyGo Bubble Humidifier	1425-1014	FDA UDI	Class I	Active
Disposable Anesthesia Circuit	9577	FDA UDI	Class I	Unknown
Respiratory Adaptor W/Luer Port, Cap	0400	FDA UDI	Class I	Unknown
Pulset	3302-91VT	FDA UDI	Class I	Unknown
Circulaire II Aerosol Drug Delivery System	0339	FDA UDI	Class II	Active
Uni-Lim 84" Adult Coaxail Breathing Circuit	9030	FDA UDI	Class I	Active
Pulset	3103-95	FDA UDI	Class I	Unknown
Hyperinflation	7-N7905	FDA UDI	Class II	Active
OxyGo Oxygen Tubing	1425-1008	FDA UDI	Class I	Active
Transport Kit with Adult Elongated Oxygen Mast	9439	FDA UDI	Class I	Active
Disposable Anesthesia Breathing Circuit	8625	FDA UDI	Class I	Unknown
Muc-Away	0493	FDA UDI	Class II	Active
Disposable Anesthesia Breathing Circuits	9196	FDA UDI	Class II	Unknown
A-Line	3100-20	FDA UDI	Class I	Active
Pulset	3105	FDA UDI	Class I	Active
Cannula, Adult High Flow	0550	FDA UDI	Class I	Unknown
Bacterial Viral Filter	6378	FDA UDI	Class II	Unknown
Disposable Anesthesia Circuits	8047	FDA UDI	Class I	Unknown
BlockAide Pulmonary Function Filter	6901-1E	FDA UDI	Class II	Active
"Mini Muc"	0488	FDA UDI	Class II	Active
Disposable Anesthesia Circuits	9328	FDA UDI	Class II	Active
Pulset	3303	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.