Vive MOB1106BLKRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810113577173), received between Aug 13, 2026 and Aug 13, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Collapse” (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.

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, 2026Collapse

  A customer reported an injury involving the use of a rollator walker. According to the initial report, the customer was being pushed by another individual while seated on the device in a parking lot area. When the walker encountered an uneven surface or bump transitioning from the parking lot to the sidewalk, the device reportedly collapsed, causing the customer to fall backward and strike the back of their head on the asphalt. The customer also reported additional minor injuries, including scrapes, and indicated that the assisting individual sustained a leg injury during the incident.The customer sought medical evaluation in the emergency room, where imaging (X-rays and CT scan) was performed to rule out serious complications.It is important to note that communication with the customer has ceased, and no further details or clarification have been obtained since the initial report.Additionally, the product's instruction manual clearly states: "Do not push a person seated on the rollator. The rollator is a walking aid only and not to be used as a transportation device." Based on the information provided, the device appears to have been used in a manner inconsistent with its intended

  Patient problems: Concussion

  MAUDE report 50234782 ↗