Permobil M Corpus VSRecalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 17330818002003), received between Sep 13, 2023 and Aug 11, 2026 — classified as 5 injuries.

The most frequently reported specific device problem is “Use of Device 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryAug 11, 2026Adverse Event Without Identified Device or Use Problem

  Reports while operating the device inside the home, while turning to maneuver down a hallway, the end-user reportedly drove the device into a wall where their arm became entrapped between the armrest and wall resulting in an injury requiring medical intervention.

  Patient problems: Bone Fracture(s); Limb Fracture

  MAUDE report 50211934 ↗
• InjuryApr 1, 2026Adverse Event Without Identified Device or Use Problem

  RECEIVED REPORT CLAIMING THE RETRACTABLE PANEL HOLDER, WHEN ROTATED INWARDS, WOULD ALLOW THE JOYSTICK TO CONTACT THE TRAY MOUNTING HARDWARE AND THIS WOULD ENGAGE AN INVOLUNTARY DRIVE COMMAND. REPORTS ON ONE INSTANCE, THE CHAIR WAS INADVERTENTLY DRIVEN INTO A WALL WHERE THE END-USER SUSTAINED A FRACTURE TO THEIR ANKLE.

  Patient problems: Bone Fracture(s); Limb Fracture

  MAUDE report 24757557 ↗
• InjuryJan 15, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  RECEIVED REPORT CLAIMING THE END-USER WAS FOUND IN THEIR ROOM, ON THE FLOOR, AFTER HAVING FALLEN OUT OF THE DEVICE SEATING. THIS EVENT RESULTED IN AN INJURY REQUIRING MEDICAL INTERVENTION TO ADDRESS.

  Patient problems: Bone Fracture(s); Limb Fracture

  MAUDE report 21162257 ↗
• InjuryMar 1, 2024Use of Device Problem; Use of Device Problem

  REPORTS WHILE END-USER WAS NAVIGATING THEIR POWER WHEELCHAIR THROUGH A RESTAURANT, THE END-USERS FOOT CAUGHT THE CORNER OF A WALL FORCING THEIR LEG TO ROTATE BACKWARD. THIS EVENT RESULTED IN AN INJURY REQUIRING MEDICAL INTERVENTION TO ADDRESS.

  Patient problems: Bone Fracture(s)

  MAUDE report 18822447 ↗
• InjurySep 13, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  REPORT RECEIVED WHILE CONDUCTING AN EVALUATION FOR A STANDING WHEELCHAIR, THE END-USER REPORTEDLY SUSTAINED AN INJURY TO THEIR LEG WHICH REQUIRED MEDICAL INTERVENTION TO ADDRESS.

  Patient problems: Bone Fracture(s); Limb Fracture

  MAUDE report 17740974 ↗