Westmed, Inc. recalls
Every recall we track for Westmed, Inc. — 10 in all, from 2019–2024 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Westmed, Inc. peaked in 2020 (6); 10 since 2017. 10% rated “stop using now”.
All FDA recall records for Westmed, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 1 | 2 | 0 | 3 |
| 2020 | 0 | 6 | 0 | 0 | 6 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 1 | 0 | 0 | 0 | 1 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Westmed, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Westmed, Inc. recalls
3 shown- Stop using nowMedical device
Westmed, Inc. recalls 1) 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 recalls two types of flex extenders due to connector issues that may cause leaks or disconnections, risking serious injury or death during medical use.
WestmedSep 27, 2024 - Use cautionMedical device
Westmed, Inc. recalls REF 0562, Adult Elongated O2/CO2 Mask, 10'X0.50 GSL w/ Swivel Elbow, 2" Pigtail w/Female Luer Connectors, 7' Oxygen
Westmed recalls adult oxygen/CO2 masks with potential loose connections causing delayed treatment. Affected units have specific model and lot numbers.
WestmedNov 11, 2020 - Lower riskMedical device
Westmed, Inc. recalls Neo-Vent Infant T-Piece Resuscitation Circuit With Infant Mask; Circuit for use on compatible Infant Resuscitators.
Westmed recalls Neo-Vent Infant T-Piece Resuscitation Circuits with 15mm OD connections that may not fit infant resuscitators. Affected units have specific model numbers and were sold in 2018.
WestmedJan 15, 2019
Westmed, Inc. recall questions
How many recalls has Westmed, Inc. had?
10 recalls from Westmed, Inc. are on record with U.S. safety agencies, from 2019–2024.
What is the most recent Westmed, Inc. recall?
Westmed, Inc. recalls 1) 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, dated Sep 27, 2024. Every Westmed, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Westmed, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Westmed, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.