BARIATRIC POWER POSITIONING SYSTEM BPPS-TRecalls & reported problems
Motion Concepts Inc · DROP SEAT - MAXX RAIL · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07540147011406), received between Mar 31, 2022 and Mar 31, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Unintended System Motion” (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
Device problems
- Unintended System Motion1
Patient problems
- Bruise/Contusion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 31, 2022Unintended System Motion; Unintended System Motion
ON 21-MAR-2022, MOTION CONCEPTS LP WAS NOTIFIED BY MEDBLOC INC. (MOTION CONCEPTS IMPORTER), THAT ONE OF THEIR DEALERS (FONTE SURGICAL SUPPLY, ROCHESTER, NY) INFORMED THEM OF AN INCIDENT THAT TOOK PLACE ON (B)(6) 2022. THE DEALER REPORTED THAT, THE SYSTEM STARTED TO TILT ON IT OWN, WHILE THE END USER WAS SITTING ON THE WHEELCHAIR. THE END USER TRIED TO TURN OFF THE TILTING MECHANISM BUT HAD NO SUCCESS. THE END USER GOT HIT ON THE COUNTERTOP, CAUSING BRUISING ON THE SHINS AND LEGS ON BOTH SIDES.
Patient problems: Bruise/Contusion
MAUDE report 13971057 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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