Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Sprint 200 wheeled stretcher Recalled by Linet Spol. S.r.o. Due to Labeling being updated to assure user is securing...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Linet Spol. S.r.o. directly.
Affected Products
Sprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and 1ES211-1.
Quantity: 335 stretchers (310 US, 25 OUS)
Why Was This Recalled?
Labeling being updated to assure user is securing the siderail to a locked position to prevent potential patient fall and injury.
Where Was This Sold?
This product was distributed to 14 states: AL, CA, FL, IA, KY, LA, MN, NV, NC, OK, TX, VA, WA, WV
About Linet Spol. S.r.o.
Linet Spol. S.r.o. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report