TRZ-CG POWER POSITIONING SYSTEM 45BT-MAXXRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00754014710423), received between Mar 2, 2022 and Mar 2, 2022 — 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.

• MalfunctionMar 2, 2022Mechanical Problem; Mechanical Problem

  ON 02-FEB-2022, (B)(4), WHO IS REPRESENTING MOTION SPECIALTIES & MOTION GP EMAILED, AND NOTIFIED US ABOUT AN INCIDENT THAT TOOK PLACE ON (B)(6) 2018. AS PER THE PLAINTIFF'S CLAIM, THE REPORTED WHEELCHAIR WAS PURCHASED BY THE END-USER IN 2018 AND ON (B)(6) 2018, THE WHEELCHAIR MALFUNCTIONED AND THE LOCKING MECHANISM HOLDING THE CHAIR IN SEATED POSITION FAILED, CAUSING THE END-USER FELL OUT FROM THE WHEELCHAIR BY HITTING HIS HEAD AND LEFT SHOULDER. AS THE END-USER WAS IMMOBILE AND REQUIRES 24 HOURS CARE, HE WAS BED RIDDEN WITHOUT THE USE OF FUNCTIONING WHEELCHAIR FOR UNSPECIFIED TIME. THE PLAINTIFF'S CLAIM ALSO MENTIONS THAT THE END-USER DEVELOPED A PRESSURE ULCER FROM HAVING TO USE HIS OLD WHEELCHAIR AS THE SEAT OF THIS OLD WHEELCHAIR WAS WORN AND INEFFECTIVE. DUE TO THE ULCER, THE END-USER'S RELATIVE HAS TO DO FURTHER DIFFICULT PHYSICAL CARE AND THE END-USER SUFFERED DEPRESSION, ANXIETY AND 15-MONTH BEDREST WITHOUT WHEELCHAIR, WITH FURTHER MEDICAL ATTENTION NEEDED FOR HIS ULCER AND OTHER HEAD/SHOULDER INJURY.

  Patient problems: Anxiety; Depression; Fall; Ulcer

  MAUDE report 13652820 ↗