Westmed recalls

Westmed has 24 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 6 Nov 2024. 1 is still ongoing.

Total recalls24since 2012

Last 12 months0reported

Class I00% of total

Ongoing1latest 6 Nov 2024

Recalls per month, last 24 months

click a bar for that month

0Oct '24 1 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 24 100%Class III 0 0%

Why westmed is recalled

Product types

By year

202414%
2021625%
2020313%
20121458%

Ongoing westmed recalls

1 active

Reported	Class	Recall	Company	Reason	Where
6 Nov 2024Device	CLASS II	Flex Extenders, 2" OD ID recalled by Westmed	Westmed	Foreign Material	30 states

All westmed recalls, newest first

24 total

Reported	Class	Recall	Company	Reason	Where
6 Nov 2024Device	CLASS II	Flex Extenders, 2" OD ID recalled by Westmed	Westmed	Foreign Material	30 states
6 Jan 2021Device	CLASS II	Disposable Respiratory Products Non-rebreather Mask recalled by Westmed	Westmed	Other	Nationwide
6 Jan 2021Device	CLASS II	REF 0562F, Adult CO2/O2 Mask, 10'X0.50 GSL w/ Swivel Elbow, 2" recalled	Westmed	Other	Nationwide
6 Jan 2021Device	CLASS II	REF 3102-E, Elongated Oxygen Mask, Adult Oxygen Elongated Mask recalled	Westmed	Other	Nationwide
6 Jan 2021Device	CLASS II	REF 0930 Adult Elongated CO2/O2 Mask, 7' Tubing w/ Threaded Nut recalled	Westmed	Other	Nationwide
6 Jan 2021Device	CLASS II	REF 0562K (Adult Elongated O2/CO2 Mask - Product Usage: intended to recalled	Westmed	Other	Nationwide
6 Jan 2021Device	CLASS II	REF 0562, Adult Elongated O2/CO2 Mask, 10'X0.50 GSL w/ Swivel Elbow recalled	Westmed	Other	Nationwide
8 Jul 2020Device	CLASS II	Neo-Vent Infant T-Piece Resuscitation Circuit With Neonatal Mask recalled	Westmed	Mold	Nationwide
8 Jul 2020Device	CLASS II	Neo-Vent Infant T-Piece Resuscitation Circuit;Circuit recalled	Westmed	Mold	Nationwide
8 Jul 2020Device	CLASS II	Neo-Vent Infant T-Piece Resuscitation Circuit With Infant Mask recalled	Westmed	Mold	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.