NA 211083Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10886705001569), received between Jul 24, 2019 and Jan 20, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Degraded” (3 reports).

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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 20, 2026Degraded

  IT WAS REPORTED THAT DURING AN UNSPECIFIED SURGICAL PROCEDURE IT WAS OBSERVED THAT THE MINI DRBIT 2.1MM DEVICE WAS NOT SHARP ENOUGH. IT WAS REPORTED THAT THE PRODUCT WAS USED AS IS AND THE SURGERY WAS COMPLETED SUCCESSFULLY. THERE WAS NO SURGICAL DELAY AND NO HARM TO THE PATIENT. NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24123104 ↗
• MalfunctionApr 9, 2025Degraded; Degraded

  IT WAS REPORTED THAT DURING AN UNSPECIFIED SURGICAL PROCEDURE THE MINI DRBIT 2.1MM EA DEVICE DRILL BIT BECAME WEAKENED. THE SURGEON MENTIONED THAT THE DRILL BIT SHOULD NOT BE WEAK BECAUSE IT WAS A DELICATE SURGERY AND THE DRILL BIT COULD NOT BE PRESSED AGAINST THE AFFECTED AREA. THERE WAS NO DELAY IN THE PROCEDURE REPORTED. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21809635 ↗
• MalfunctionApr 7, 2025Degraded; Degraded

  IT WAS REPORTED THAT DURING AN UNKNOWN SURGERY PERFORMED, IT WAS OBSERVED THAT THE MINI DRBIT 2.1MM DEVICE BECAME WEAKENED. THERE WAS NO DELAY IN THE PROCEDURE REPORTED. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21784822 ↗
• MalfunctionJul 24, 2019Dull, Blunt; Failure to Cut; Dull, Blunt; Failure to Cut

  IT WAS REPORTED THAT THE SURGEON RECOGNIZED THAT THE DRILL TIP (P/N AND LOT# WERE UNKNOWN) WAS DULL, SO THAT THE SURGEON COULD NOT CREATE PILOT HOLE FOR MINI QUICK ANCHOR PLUS (P/N AND LOT# WERE UNKNOWN) DURING THE SURGERY ON (B)(6) 2019. THE SURGERY WAS FINISHED WITHOUT ANY OTHER PROBLEM ALTHOUGH IT WAS NOT REPORTED HOW THE SURGERY WAS COMPLETED. IT WAS BRAND NEW AND THE FIRST USE WHEN THE ISSUE OCCURRED. THERE WAS NO INFORMATION OF SURGICAL DELAY AND NO HARM TO THE PATIENT. NO FURTHER INFORMATION WAS PROVIDED BY THE HOSPITAL. ADDITIONAL INFORMATION PROVIDED BY AFFILIATE REPORTING A MINI QUICK ANCHOR WAS USED DURING THE PROCEDURE BUT THE LOT NUMBER IS UNKNOWN.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8824376 ↗