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PINNACLE GRIPTION TF 2217-01-517Recalls & reported problems

Depuy (Ireland) · PINNACLE GRIPTION TF RASPING POWER ADAPTOR · Class 1

Data updated Oct 18, 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 10603295097976), received between Dec 8, 2021 and Dec 8, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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

  • Break1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • MalfunctionDec 8, 2021Break; Break

    SURGEON WAS USING THE GRIPTION AUGMENTS DURING A TOTAL HIP. WHEN USING THE RASPING POWER ADAPTER (CONNECTED TO STRYKER POWER) TO REAM THE ACETABULUM, THE ADAPTER BROKE AND WAS NO LONGER FUNCTIONAL. SURGERY WAS DELAYED A FEW MINUTES WHILE THEY INSPECTED THE ADAPTOR, WHICH WAS DETERMINED TO BE BROKEN AND NON FUNCTIONAL. THIS OCCURRED INTRA OP BUT SURGERY WAS COMPLETED SUCCESSFULLY WITH NO PATIENT ISSUES. ITEM HAS BEEN DISCARDED AND THEREFORE NO LOT # AVAILABLE. NO FURTHER INFORMATION IS AVAILABLE. WAS SURGERY DELAYED DUE TO THE REPORTED EVENT? YES, IF YES, NUMBER OF MINUTES: 2, WAS PROCEDURE SUCCESSFULLY COMPLETED? YES, WERE FRAGMENTS GENERATED? NO, IF YES, WERE THEY REMOVED EASILY WITHOUT ADDITIONAL INTERVENTION? UNKNOWN, PATIENT STATUS/ OUTCOME / CONSEQUENCES NO, WAS OTHER MEDICAL INTERVENTION (E.G. X-RAYS, ADDITIONAL PROCEDURES, PRESCRIPTIONS, OTC, REVISION) REQUIRED: UNKNOWN, IS THE PATIENT PART OF A CLINICAL STUDY? UNKNOWN, (B)(4), DEVICE PROPERTY OF NONE, DEVICE IN POSSESSION OF NONE BY CHECKING THIS BOX I CERTIFY THAT ALL INFORMATION THAT ARE KNOWN/AVAILABLE HAS BEEN DISCLOSED. IF ANY NEW INFORMATION WILL BE MADE AVAILABLE, THE ADDITIONAL INFORMATION WILL BE SUBMITTED THROUGH

    Patient problems: Insufficient Information

    MAUDE report 12960957 ↗

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Sources and updates

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