Vive MOB1019PNKRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00818323024937), received between Jan 27, 2025 and Jan 27, 2025 — classified as 2 injuries.

The most frequently reported specific device problem is “Mechanical Problem” (2 reports).

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJan 27, 2025Mechanical Problem; Mechanical Problem

  THE CUSTOMER RECENTLY HAD FOOT SURGERY, AND WHILE USING THE ITEM, SHE FELL AND HIT THE FOOT THAT UNDERWENT SURGERY. SHE REPORTS THAT THIS HAPPENED BECAUSE THE ITEM IS TOO UNSTABLE AND DANGEROUS.

  Patient problems: Hemorrhage/Blood Loss/Bleeding

  MAUDE report 21241187 ↗
• InjuryJan 27, 2025Mechanical Problem; Mechanical Problem

  THE COMPANY ALREADY REPLACED THE FAULTY UNIT WITH ONE IN STOCK, SHE WAS ABOUT TO USE THE KNEE WALKER UNTIL THE BREAKS FAIL AND SHE FELT DOWN, WHEN HIS HUSBAND TRY TO PICK HER UP AND SEE WHAT HAPPENED HE END ALSO FALLING DOW. THEY DECIDE NOT GOING INTO THE HR BUT SHE HAS BRUISES.

  Patient problems: Hemorrhage/Blood Loss/Bleeding

  MAUDE report 21241183 ↗