VIVE MOB1014BLKRecalls & reported problems
Vive Health LLC · Forearm Crutches Black · 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 00818323027198), received between Aug 29, 2019 and Aug 29, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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.
Most reported problems
Device problems
- Break1
- Collapse1
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.
InjuryAug 29, 2019Break; Collapse
CONSUMER LEFT A COMMENT STATING, "I GOT THESE YESTERDAY. WENT OUT TODAY AND THE ONE CRUTCHES COLLAPSED ON ME, MAKING ME FALL TO THE GROUND AND INJURING MYSELF. THE REASON I GOT THESE IS BECAUSE MY OLD ONES DID THE SAME THING. THESE WILL BE GOING BACK." FDA SAFETY REPORT ID# (B)(4).
Patient problems: Fall
MAUDE report 8949605 ↗
Other Crutch devices
- SPATIAL FRAME 71070365Smith & Nephew, Inc. · CRUTCH3 reports
- CARDINAL HEALTH CA901YTHCardinal Health 200, LLC · CRUTCH1 report
- DRIVEMEDICAL 10402-8Drive Devilbiss Healthcare · CRUTCH1 report
- CARDINAL HEALTH CA901TLCardinal Health 200, LLC · CRUTCH1 report
- Walgreens 783180Drive Devilbiss Healthcare · CRUTCH1 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 · 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.
How reports and recalls are matched · Editorial policy · Report an error on this page