VIVE MOB1026Recalls & reported problems
Vive Health LLC · Tri-Rollator · Class 1
- 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 00818323027952), received between Oct 21, 2025 and Oct 21, 2025 — 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Unintended Movement1
Patient problems
- Bone Fracture(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 21, 2025Unintended Movement; Unintended Movement
THE CUSTOMER EXPERIENCED A FALL AND FRACTURED HER FIBULA. SHE REQUIRED SURGERY FOLLOWED BY PHYSICAL THERAPY. THE INCIDENT OCCURRED AS SHE WAS TURNING THE CORNER FROM HER KITCHEN TO HER BATHROOM, WHERE SHE LOST HER BALANCE
Patient problems: Bone Fracture(s)
MAUDE report 23348845 ↗
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- Drive R728BLDrive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.