Linet Spol. S.r.o Sprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and recall — FDA Z-1211-2023
Labeling being updated to assure user is securing the siderail to a locked position to prevent potential patient fall and injury.
Overview of recall records associated with Linet Spol. S.r.o., including dates, categories and classifications where available.
Classification mix: Class II: 3.
Labeling being updated to assure user is securing the siderail to a locked position to prevent potential patient fall and injury.
A component used within the side rail mechanism may malfunction, resulting in the side rail either not locking properly in the upper position or the side rail becoming stuck in the upper…
LINET has recently become aware of a potential safety issue for the AVE 2 Birthing Bed caused by the power cable breaking at the bed connection or the orange insulation of the power cable…
This page summarizes recall records in which the official source identifies Linet Spol. S.r.o. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.