# FDA recall Z-1211-2023

> **Linet Spol. S.r.o.** · Class II · device recall initiated 2023-01-18.

## Product

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.

## 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.

## Key facts

- **Recall number:** Z-1211-2023
- **Recalling firm:** Linet Spol. S.r.o.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-01-18
- **Report date:** 2023-03-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Zelevcice, Czech Republic

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1211-2023

## Citation

> AI Analytics. FDA recall Z-1211-2023. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1211-2023. Source: US FDA. Licensed CC0.

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