Home / Recalls / Medical Devices
Linet Spol. S.r.o. recalls Sprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and 1ES211-1.
Recalled March 15, 2023 · FDA recall Z-1211-2023 · Linet Spol. S.r.o
Hazard
Labeling being updated to assure user is securing the siderail to a locked position to prevent potential patient fall and injury. · FDA Class II
Units
335 stretchers (310 US, 25 OUS)
Sold at
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 Canada.
Description
Labeling being updated to assure user is securing the siderail to a locked position to prevent potential patient fall and injury.
Product
Sprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and 1ES211-1.
Manufacturer(s)
Linet Spol. S.r.o.
Made in
Czech Republic
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →