MODULAR POWER POSITIONING SYSTEM 45T-12L-RPSB-MAXXRecalls & reported problems
Motion Concepts Inc · DROP SEAT - MAXX RAIL · Class 2
All models of MODULAR POWER POSITIONING SYSTEM (7)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00754014710119), received between May 24, 2018 and May 24, 2018 — classified as 2 injuries.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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
Device problems
- Improper or Incorrect Procedure or Method1
- Misassembly by Users1
- Use of Device Problem1
Patient problems
- Injury2
- Abrasion1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 24, 2018Improper or Incorrect Procedure or Method; Misassembly by Users; Improper or Incorrect Procedure or Method; Misassembly by Users
ON (B)(6) 2018, MOTION CONCEPTS WAS INFORMED BY (B)(6) (MOTION CONCEPTS IMPORTER), THAT ONE OF THEIR DEALERS AT (B)(6), WAS NOTIFIED OF AN INCIDENT THAT TOOK PLACE ON (B)(6) 2018. THE DEALER REPORTED THAT THE END USER GOT A CUT ON HER CALF WHILE THE END USER'S HUSBAND WAS TRYING TO BACK HER UP FROM THE TABLE SHE WAS AT. THE JOYSTICK, WHICH WAS RETRACTED WHILE HER HUSBAND WAS BACKING HER UP, GOT ACTIVATED THAT CAUSED THE SYSTEM TO TURN AND THE CENTER MOUNT OF THE SYSTEM ENDED UP CUTTING HER CALF. MEDICAL ATTENTION WAS NEED FOR THE END USER AS THERE WAS BLEEDING ON HER CALF. ACCORDING TO THE DEALER, THE END USER WANTS MODIFICATION ON THE CHAIR.
Patient problems: Abrasion; Injury
MAUDE report 7542038 ↗InjuryMay 24, 2018Use of Device Problem
MEDBLOC GOT NOTIFIED BY ONE OF THEIR DEALERS AT (B)(6) ON (B)(6) 2018 ABOUT AN INCIDENT THAT TOOK PLACE ON (B)(6) 2018. THE DEALER REPORTED THAT THE END USER GOT A CUT ON HER CALF WHILE THE END USER'S HUSBAND WAS TRYING TO BACK HER UP FROM THE TABLE SHE WAS AT. THE JOYSTICK, WHICH WAS RETRACTED WHILE HER HUSBAND WAS BACKING HER UP, GOT ACTIVATED THAT CAUSED THE SYSTEM TO TURN AND THE CENTER MOUNT OF THE SYSTEM ENDED UP CUTTING HER CALF. MEDICAL ATTENTION WAS NEED FOR THE END USER AS THERE WAS BLEEDING ON HER CALF. ACCORDING TO THE DEALER, THE END USER WANTS MODIFICATION ON THE CHAIR.
Patient problems: Injury
MAUDE report 7541314 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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