PLR2985MRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00606509401289), received between Feb 18, 2020 and Mar 16, 2026 — classified as 3 injuries.

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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryMar 16, 2026Appropriate Device Problem Term/Code Not Available

  CONSUMER'S HUSBAND ALLEGES THAT HIS WIFE SLIPPED OUT OF THE CHAIR AND FELL TO THE FLOOR. SHE WAS VERY WEAK DUE TO SEVERE ANEMIA.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24604196 ↗
• InjuryFeb 21, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  CONSUMER'S WIFE ALLEGES THE CHAIR ALLEGEDLY THREW HER HUSBAND OUT OF IT AND CALLED 911 TO HELP HIM UP.

  Patient problems: Bruise/Contusion

  MAUDE report 9738198 ↗
• InjuryFeb 18, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ALLEGES THERE WAS A DIP IN THE BACK LEFT SIDE OF THE CHAIR. PROVIDER INSTALLED MORE STUFFING BUT CUSTOMER ALLEGES THIS MADE THE ISSUE WORSE AND IS SLIPPING DOWN FROM THE BACK.

  Patient problems: Discomfort

  MAUDE report 9720127 ↗