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PINNACLE HD SL600Recalls & reported problems

Harmar Summit, LLC · PINNACLE HD NON-KEYED · 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 00817650022395), received between Jul 20, 2018 and Jul 20, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Component Misassembled” (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

  • Component Misassembled1

Patient problems

  • Pain1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 20, 2018Component Misassembled; Component Misassembled

    ON (B)(6) 2018 THE USER GOT ON THE STAIR LIFT CHAIR AT THE BOTTOM STEP AND WAS RIDING UPWARDS TO THE TOP LANDING WHEN THE STAIR LIFT MADE A POPPING SOUND AND THE STAIR LIFT SEAT/CHASSIS DESCENDED BACK DOWN THE STAIRCASE TO THE END OF THE RAIL. THE USER STEPPED OFF THE STAIR LIFT AS IT DESCENDED AND SUSTAINED MINOR PAIN IN HER LEG AND A SMALL CUT ON HER FINGER.

    Patient problems: Pain

    MAUDE report 7705796 ↗

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Sources and updates

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