Pinnacle Pinnacle, Rave, LeafRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00817650026188), received between Feb 18, 2026 and Mar 6, 2026 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Damaged Thread” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryMar 6, 2026Installation-Related Problem

  IT WAS REPORTED THAT WHEN THE END USER WAS RIDING THE PINNACLE SL300 UP THE STAIRS, THE CHAIR DESCENDED ABRUPTLY NEAR THE TOP OF THE STAIRCASE, THRUSTING THE USER ONTO THE FLOOR. IT WAS ALSO REPORTED THAT THE END USER EXPERIENCED HUMERAL, RIB, AND ANKLE FRACTURES AND A DEGLOVED LOWER RIGHT LEG REQUIRING HOSPITALIZATION AND HAD SURGERY TO REDUCE THE ANKLE FRACTURE. THE REPORTER STATED THAT THE SL300 WAS INSTALLED AT THE END USER'S RESIDENCE ON (B)(6) 2025, AND THE EVENT HAPPENED APPROXIMATELY 30 MINUTES AFTER THE INSTALLATION.

  Patient problems: Bone Fracture(s); Fall

  MAUDE report 24537763 ↗
• MalfunctionFeb 18, 2026Damaged Thread

  IT WAS REPORTED THAT WHEN THE END USER WAS RIDING THE PINNACLE SL300 DOWNSTAIRS, THE TRACK'S END CAP FELL OFF AND SEVEAL PIECES OF THE GEAR RACK SLIDE OUT TOWARDS THE BOTTOM OF THE STAIRCASE. THE REPORTER STATED THAT THE END USER CONTINUED TO DESCEND A FEW FEET AND HIT HER WRIST AGAINST THE ARMREST CAUSING THE BRUISING. THE SL300 UNIT WAS INSTALLED IN (B)(6) 2025.

  Patient problems: Bruise/Contusion

  MAUDE report 24381533 ↗