R82 Crocodile, size 2Recalls & reported problems
R82 A/S · Class 1
Data updated Oct 16, 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 05707292355959), received between Mar 30, 2026 and Mar 30, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Mechanical Problem” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Mechanical Problem1
Patient problems
- Fall1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 30, 2026Mechanical Problem
THE END USER'S MOTHER CLAIMS THAT THE WAIST BELT SNAPPED OFF WHILE HE WAS WALKING. WHILE WALKING, THE WAIST BELT SNAPPED OFF AND HE FELL FACE FIRST ONTO CONCRETE. HE LOST A TOOTH AND MAY NEED STITCHES IN HIS LIP. NEED TO SEE DENTIST AND THERE IS A CONCERN THAT IT MAY HAVE DAMAGED HIS PERMANENT TEETH.
Patient problems: Fall
MAUDE report 24714253 ↗
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- Drive 10257RD-1Drive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- Drive R728BLDrive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- Drive R726BKDrive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- Drive 10215BL-1Drive Devilbiss Healthcare · WALKER, MECHANICAL8 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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