Panacea 1000 PAN1000-FLEX-RILQSRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810055884223), received between Jul 23, 2025 and Jul 23, 2025 — classified as 1 malfunction.

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. What reports can and can't tell you · How this data works · Data updated Oct 18, 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.

• MalfunctionJul 23, 2025Mechanical Problem; Mechanical Problem

  IT WAS REPORTED TO THE MANUFACTURER, BY THE END USER, PER THE END USER, THE FOLLOWING OCCURRED ON THE EVENING ON (B)(6) 2025: ALLEGEDLY, THE RESIDENT WAS IN BED AND WAS RAISING THE HEAD UP. PER (B)(6), THE HEAD WAS ONLY ABOUT HALFWAY UP WHEN THERE WAS AN ALLEGED LOUD POPPING NOISE AND THE WHOLE HEAD OF THE BED DROPPED DOWN. THERE WERE NO INJURIES ACCORDING TO THE FACILITY. COMPLAINT #(B)(4) WAS ENTERED INTO OUR SYSTEM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22579416 ↗