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Open, Classified

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

FDA Recall Z-1211-2023 · Posted 2023-03-04

Recalling FirmLinet Spol. S.r.o.
Recall StatusOpen, Classified
Product CodeFPO
Date Initiated2023-01-18
Product Quantity335 stretchers (310 US, 25 OUS)

Reason for Recall

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

Firm Action

The firm issued "URGENT MEDICAL DEVICE CORRECTION" recall letters dated 1/17/2023 via email on 1/18/2023. The letter explains the issue that an audible clicking sound can be heard when the side rail is raised, but this sound does not indicate the side rail has locked into the raised position. The consignee is to take immediate action to notify caregivers using the Sprint 200 of this potential hazard and proper use for securing a side rail in the raised position. The consignee is informed that Linet will be adding additional safety warning labels located at each side rail latch (2 per side of stretcher), add additional safety warning labels to both side rails (1 per side of stretcher), and that additional training material and an updated copy of the Sprint 200 Emergency Stretcher Instructions for Use and Technical Description manual is available using the QR code in the letter or by following a link to access the materials. The firm's service department will be contacting the consignees to schedule an appointment to perform the corrections. Photos of the additional warning labels are included in the letter. Please contact LINET service department at 877-815-9897 with immediate questions or concerns.

Root Cause

Labeling design

Distribution Pattern

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.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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