DRIVEMEDICAL AM171AMRecalls & reported problems
Drive Devilbiss Healthcare · Rollators3-Wheel Product Description: Amer 3wheeled rollator w/Bag&basket 1/ea · Class 1
All models of DRIVEMEDICAL (111)
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 00822383548388), received between Sep 3, 2021 and Sep 3, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Material Fragmentation” (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
- Material Fragmentation1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 3, 2021Material Fragmentation; Material Fragmentation
DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A ROLLATOR. THE DEVICE HAS NOT BEEN RETRIEVED FOR EVALUATION. WE ARE FILING THIS REPORT IN AN OVERABUNDANCE OF CAUTION. WE WILL FILE A FOLLOW-UP ID ADDITIONAL DATA BECOMES AVAILABLE. WHILE IN USE THE FRONT WHEEL OF THE DEVICE BROKE OFF. THE END-USER FELL. WE HAVE NOT RECEIVED CONFIRMATION OF INJURIES THAT HER ATTORNEY LABELED "LIFE ALTERING". USER WAS RECOVERING FROM HIP REPLACEMENT SURGERY. HER SURGEON ADVISED HER THAT THE HIP REPLACEMENT IS FINE. HOWEVER SHE WAS EXPERIENCING NECK AND BACK PAIN, AND MAY HAVE BROKEN HER NOSE.
Patient problems: Insufficient Information
MAUDE report 12422696 ↗
Other WALKER, MECHANICAL devices
- Drive 10257BL-1Drive Devilbiss Healthcare · WALKER, MECHANICAL13 reports
- Drive R726RDDrive Devilbiss Healthcare · WALKER, MECHANICAL1 death10 reports
- Drive 790Drive Devilbiss Healthcare · WALKER, MECHANICAL10 reports
- Drive R728BLDrive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- Drive 10257RD-1Drive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- DRIVEMEDICAL 795BDrive 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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