BARIATRIC POWER POSITIONING SYSTEM BPPS-T-RESRRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00754014711413), received between Oct 1, 2019 and Nov 20, 2020 — classified as 2 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 16, 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.

• InjuryNov 20, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  ON 23-OCT-2020, MOTION CONCEPTS LP WAS NOTIFIED BY MEDBLOC INC. (MOTION CONCEPTS IMPORTER), THAT ONE OF THEIR DEALERS (NATIONAL SEATING & MOBILITY, (B)(4)) INFORMED THEM OF AN INCIDENT THAT TOOK PLACE ON (B)(6) 2020. THE DEALER REPORTED THAT THE END USER WAS HIT BY A BUS AND THERE WAS NO INJURY REPORTED ON THE END-USER, BUT THE WHEELCHAIR NEEDS TO REPLACE THE ENTIRE CENTER MOUNT ASSEMBLY AS IT WAS DAMAGED DURING THE ACCIDENT. THE DEALER ALSO STATED THAT THE CHAIR WAS DRIVING FINE AND NO ISSUES WERE NOTED ON THE MOTORS USED ON THE MENTIONED SYSTEM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 10877097 ↗
• InjuryOct 1, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

  ON 06-SEP-2019, MOTION CONCEPTS LP WAS NOTIFIED BY MEDBLOC INC (THE MOTION CONCEPTS USA IMPORTER) THAT ONE OF MEDBLOC'S DEALERS (VAMC-PHILADELPHIA, PA) WAS NOTIFIED OF AN INCIDENT THAT TOOK PLACE ON (B)(6) 2019. THE DEALER REPORTED THAT THE END USER STATED THAT HE WAS RIDING DOWN THE ROAD AND HIT A BUMP. AFTER HITTING THE BUMP, THE SYSTEM "STARTED TILTING ON ITS OWN". HE ATTEMPTED TO GET OUT OF THE SYSTEM AND FELL TO THE GROUND INJURING HIS HEAD. HE STATED HE AND THE SYSTEM WERE BROUGHT TO AN EMERGENCY ROOM WHERE THEY PERFORMED AN EKG SINCE HE IS AN EXISTING HEART PATIENT. NO X-RAY TO HIS HEAD OR BACK AND NO STITCHES WERE REQUIRED. HE WAS SENT HOME WITH THE CHAIR AND THEN CONTACTED US. THE END USER SAID THAT THE SYSTEM DISPLAY SCREEN INDICATED THAT "SWITCH MAY BE STUCK" .THE END USER REMOVED THE 8-WAY SWITCH AND THE USER COULD OPERATE THE SEATING SYSTEM AS INTENDED.

  Patient problems: Head Injury

  MAUDE report 9142033 ↗