PINNACLE GRIPTION 1217-20-354Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295009740), received between Aug 27, 2021 and Aug 27, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Insert” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 27, 2021Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT THE 5.0 NON-LOCKING SCREW WAS USED IN A 54/56 X20 MM GRIPTION TF AUGMENT TO COMPRESS BUT WAS ABLE TO PASS ALMOST COMPLETELY THROUGH THE FLAT (OUTER) PORTION OF THE AUGMENT. 5.5 LOCKERS WERE USED IN ADDITION TO BONE CEMENT FOR A STABLE CONSTRUCT. IT WAS ALSO INDICATED THAT THERE WAS A SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12377137 ↗