DHS 281.060SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982176554), received between Nov 12, 2024 and Nov 12, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device-Device Incompatibility” (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

Recent adverse event reports

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

• MalfunctionNov 12, 2024Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT ON AN UNKNOWN DATE, DURING AN ORIF OF A FEMUR, A DHS 6H WAS USED AND THE PLATE DID NOT SEAT ON THE T HANDLE DHS INSERTER. UNSURE WHAT WAS WRONG WITH PLATE. TSP WAS USED AND THE (B)(6) WAS USED TO BEND THE PLATE AND THE SHAFT ENDED UP BENDING AS WELL. TWO OF THE DEVICES WERE BENT. THE CABLES WERE USED AND THE CABLE LOCK WOULD NOT LOCK. ALSO, THE RATCHETING DRIVER HAD A 3.5 HEX STUCK AND UNABLE TO TAKE OUT. THERE WAS NO PATIENT STATUS, OUTCOME, OR CONSEQUENCES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20669721 ↗