VIVE MOB1033Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00818323029581), received between Jan 27, 2025 and Jan 27, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Mechanical 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. 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.

• InjuryJan 27, 2025Mechanical Problem; Mechanical Problem

  SHE RECEIVED THE PRODUCT, THEY ASSEMBLED AND WHEN SHE FIRST TRIED TO USE IT, IT TIPPED OVER AND SHE FELL WITH IT, LUCKILY SHE FELL ON HER DOG'S BED AND HAS A MINOR BRUISE SHE'S OKAY BUT IT IS EXTREMELY UNSAFE FOR HER TO USE IT. SOMEONE ELSE TREID TO USE IT AS WELL AND IT KEPT HAPPENING, THEY LOOKED AT THE PRODUCT AND IT SEEMS LIKE THE BOTTOM IS NARROWER THAN THE TOP MAKING IT UNSTABLE.

  Patient problems: Hemorrhage/Blood Loss/Bleeding

  MAUDE report 21241169 ↗