Sprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and 1ES211-1.
Reported: March 15, 2023 Initiated: January 18, 2023 #Z-1211-2023
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.
Details
- Recalling Firm
- Linet Spol. S.r.o.
- Units Affected
- 335 stretchers (310 US, 25 OUS)
- Distribution
- 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.
- Location
- Zelevcice
Frequently Asked Questions
What product was recalled? ▼
Sprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and 1ES211-1.. Recalled by Linet Spol. S.r.o.. Units affected: 335 stretchers (310 US, 25 OUS).
Why was this product recalled? ▼
Labeling being updated to assure user is securing the siderail to a locked position to prevent potential patient fall and injury.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 15, 2023. Severity: Moderate. Recall number: Z-1211-2023.
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