Sprint 200 1ES211-1Recalls & reported problems
L I N E T spol. s r.o. · The sprint stretcher transport bed with scales. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Jan 18, 2023Class IIOpen, Classified
Labeling being updated to assure user is securing the siderail to a locked position to prevent potential patient fall and injury.
Z-1211-2023 · Root cause: Labeling design · Recall details · FDA record ↗
Other Stretcher, Wheeled, Powered devices
- Prime Series 1125Stryker Corporation · STRETCHER, WHEELED, POWERED240 reports
- Prime Series 1125Stryker Corporation · STRETCHER, WHEELED, POWERED200 reports
- Prime Series 1125Stryker Corporation · STRETCHER, WHEELED, POWERED77 reports
- Prime Series 1125Stryker Corporation · STRETCHER, WHEELED, POWERED71 reports
- Sprint 200 1ES210-1L I N E T spol. s r.o. · Stretcher, Wheeled, Powered1 recall0 reports
- Prime Series 1125Stryker Corporation · Stretcher, wheeled, powered4 reports
- Electric Stretcher P8020HHill-Rom de México, S. de R.L. de C.V. · STRETCHER, WHEELED, POWERED4 reports
- Prime Series 1125Stryker Corporation · Stretcher, wheeled, powered1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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