SMALL CANNULATED SCREWS 71103232SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010623959), received between Feb 2, 2021 and Feb 2, 2021 — classified as 1 injury.

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 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.

• InjuryFeb 2, 2021Break; Break

  IT WAS REPORTED THAT DURING THE VLP FOOT PROCEDURE, A 1.1 GUIDE WAS MOUNTED ON THE MOTOR, AN X-RAY WAS TAKEN WHEN THE GUIDE WAS WELL LOCATED, A METER WAS PASSED, THEN A 2.0 CANNULATED DRILL WAS PASSED THROUGH A SCREW WITH A WASHER RING MOUNTED ON A SCREWDRIVER. AT THE TIME OF INSERTING IT, WHEN FINISHING THE ADJUSTMENT, IT WAS EVIDENT THAT THE SCREW HEAD BROKE, THE WASHER RING FELL OFF, THE SCREW REMAINED INSIDE THE PATIENT, IT COULD NOT BE REMOVED. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. THE PROCEDURE WAS FINISHED WITH A SMITH AND NEPHEW BACK UP DEVICE. NO DELAY REPORTED.

  Patient problems: Foreign Body In Patient; No Clinical Signs, Symptoms or Conditions

  MAUDE report 11269473 ↗