Linet Spol. S.r.o. recalls Sprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and 1ES211-1.
- Recall date
- January 18, 2023
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1211-2023
- FDA classification
- Class II
- Brand / firm
- Linet Spol. S.r.o.
- Sold / distributed
- US Distribution was made to AL, CA, FL, IA, KY, LA, MN, NV, NC, OK, TX, VA, WA, and WV. There was no government/military distribution. Foreign distribution was made to Australia, Bahrain, Belgium, Germany, Great Britain, Italy, Netherland, Singapore, South Africa, Switzerland, and United Emirates C…
Why it was recalled
Labeling being updated to assure user is securing the siderail to a locked position to prevent potential patient fall and injury.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Sprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and 1ES211-1.
Get recall alerts
Free email alert whenever Linet Spol. S.r.o. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Linet Spol. S.r.o.