Recall Register

Food, drugs, devices › Firms

Westmed, Inc.

FDA recalling firm · 4 enforcement events · 24 product records · 2011–2024 · AZ

Westmed, Inc. has 4 FDA enforcement events on this register (24 product records) between 2011 and 2024: 4 device; the busiest year was 2011 with 1.

0% of its events are Class I; the most common class is Class II (4). 1 event is listed as ongoing; the recalling firm's address is in AZ.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
27 Sep 20241) Flex Extenders, 5.2" x 15mm OD x 15mm ID REF S6411P 2) Flex Extender, 5.2" x 15mm OD x 22/15mm ID REF 7 5132 The Westmed Flex Extenders are non invasive, single use/disposable, large bore, corrugated plastic tubes that provide a flexible, low resistance lightweight connection between breathing circuits and patient…DeviceClass II1Ongoing
11 Nov 2020REF 3102-E, Elongated Oxygen Mask, Adult Oxygen Elongated Mask with 8' Tubing, Rx Only, CE0482, (01)00709078003172 - Product Usage: intended to connect with an oxygen source to deliver oxygen therapy to the patient.DeviceClass II6Terminated
15 Jan 2019Neo-Vent Infant T-Piece Resuscitation Circuit;Circuit for use on compatible Infant Resuscitators. 15mm OD x 10mm ID connector; REF 0415, Qty:10, Length: 60" (1.5cm), Rx Only.DeviceClass II3Terminated
18 Jan 2011Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit, Pulset, 1 cc, w/Crickett 25g x 5/8" A Needle, 25U Balanced Heparin, part number: 3165-95. An arterial blood sampling kit is a device, in kit form, used to obtain arterial blood samples from a patient for blood gas determinations.DeviceClass II14Terminated

By type and class

Device4
Class II4

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

11
13
15
17
19
21
23
25
Enforcement events for Westmed, Inc. by year initiated.

Questions and answers

How many FDA recalls has Westmed, Inc. had?

4 enforcement events (24 product records) on this register, 2011–2024: 4 device.

Are any Westmed, Inc. recalls ongoing?

1 event is listed as ongoing in the current openFDA export.

What class are Westmed, Inc. recalls?

4 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.