35A-NM Ambulance Cot 0015612Recalls & reported problems
Ferno-Washington, Inc. · 35A-NM Ambulance Cot, Non-Magnetic · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00190790000042), received between Jun 2, 2020 and Jun 2, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Unintended Movement” (1 report).
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.
Most reported problems
Device problems
- Unintended Movement1
Patient problems
- Neck Pain1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 2, 2020Unintended Movement; Unintended Movement
THE COMPLAINANT REPORTED WHILE ATTEMPTING TO RAISE THE STRETCHER WITH A PATIENT ON BOARD, THE LEGS WOULD ALLEGEDLY NOT ENGAGE. THE PATIENT ALLEGEDLY HIT THEIR HEAD ON THE NEARBY MRI EQUIPMENT AND COMPLAINED OF NECK AND HEAD PAIN, BUT DID NOT SEEK MEDICAL INTERVENTION.
Patient problems: Neck Pain; Pain
MAUDE report 10108850 ↗
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- NA 5050Stryker Corporation · STRETCHER, WHEELED1 recall99 reports
- Power-PRO 2 650700000000Stryker Corporation · STRETCHER, WHEELED2 recalls1 death42 reports
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 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- 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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