Vive Mobility MOB1057BLKRecalls & reported problems
Vive Health LLC · Rollator Model S (Black) · 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 00810113573632), received between Aug 5, 2026 and Aug 5, 2026 — 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
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 5, 2026Break
The patient reported that while using the rollator, the central hinge failed, causing him to fall to the ground and strike his head. He stated that he briefly lost consciousness for a few seconds. The patient reported that he was able to stand up and continue using the rollator afterward and did not seek medical attention.
Patient problems: Fall
MAUDE report 50141322 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.