Recall Z-1211-2023— Linet Spol. S.r.o.

Name: FDA recall Z-1211-2023
Creator: U.S. Food and Drug Administration
Published: 2023-01-18

Class II · Ongoing

Class II FDA medical device recall by Linet Spol. S.r.o., initiated 2023-01-18. FDA's recall record names no specific 510(k) clearance for this event. Product: Sprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and 1ES211-1.. Reason: Labeling being updated to assure user is securing the siderail to a locked position to prevent potential patient fall and injury..

Recalling firm: Linet Spol. S.r.o.
Classification: Class II
Status: Ongoing
Initiated: 2023-01-18
Firm location: Zelevcice, Czech Republic

Product description

Sprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and 1ES211-1.

Reason for recall

Labeling being updated to assure user is securing the siderail to a locked position to prevent potential patient fall and injury.

Data sourced from openFDA. This site is unofficial and independent of the FDA.