Vive Mobility MOB1101BLURecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810113576879), received between Aug 13, 2026 and Aug 13, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Use of Device 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.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryAug 13, 2026Use of Device Problem

  The customer reported that the wheelchair was received with the anti-tip wheels installed in the wrong position. While using the wheelchair inside his home on a tile floor, he was rolling backward when the wheelchair became caught on an object. The customer reported that when he attempted to continue moving backward, the wheelchair tipped over, causing him to fall. He reported striking his head and sustaining a fractured scapula. The customer sought medical attention in the emergency room. The customer stated that the anti-tip wheels were repositioned after the incident.

  Patient problems: Bone Fracture(s)

  MAUDE report 50234685 ↗