Linet recalls Sprint 200 wheeled stretchers with specific serial numbers due to risk of patient falls if siderail isn't locked properly. Affected units include models 1ES200-7, 1ES210-1, and 1ES211-1 with listed serial numbers.
Labeling being updated to assure user is securing the siderail to a locked position to prevent potential patient fall and injury.
Linet is recalling Sprint 200 wheeled stretchers with specific serial numbers because the siderail might not lock securely, potentially causing patient falls. This is a safety update to prevent injury during use.
The siderail on these stretchers may not lock securely in place, which could lead to the patient falling if the rail isn't properly secured. This risk exists during normal use when the equipment is not correctly maintained.
Healthcare professionals and patients using Linet Sprint 200 stretchers with the listed serial numbers are affected. Those handling the equipment without proper locking of the siderail are at higher risk.
Check for serial numbers listed in the recall: 1ES200-7 (serials starting with 20220203), 1ES210-1 (serials starting with 20220204), and 1ES211-1 (serials starting with 20220210). The UDI-DI codes 08592654358467, 08592654356685, and 08592654356678 also identify affected units.
Ensure the siderail is securely locked in place before use to prevent patient falls.
Sprint 200 wheeled stretchers with item numbers 1ES200-7, 1ES210-1, and 1ES211-1.
Check the serial numbers listed in the recall: 1ES200-7 (serials starting with 20220203), 1ES210-1 (serials starting with 20220204), and 1ES211-1 (serials starting with 20220210).
The recall does not require returning the stretcher; users should ensure the siderail is locked securely before use.
We’ve drafted a message you can send Linet to request your refund or repair — edit it as you like.
Subject: Recall Z-1211-2023 — Linet Linet Hello, I own a Linet that is covered by recall Z-1211-2023 from Linet. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
