Medline Industries, Inc. DYNJG901013BRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10195327679132), received between Nov 25, 2025 and Nov 25, 2025 — 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 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.

• InjuryNov 25, 2025Break; Break

  ACCORDING TO THE CUSTOMER, ON (B)(6) 2025 THE "DRILL BIT BROKE WHILE ATTEMPTING TO DRILL HOLES TO REPAIR CAPSULE FOR POSTERIOR HIP THROUGH BONY TUNNELS" DURING A POSTERIOR TOTAL HIP ARTHROPLASTY AND WAS LEFT IN THE PATIENT. THE CUSTOMER REPORTED "LIKELY DUE TO EXCESSIVE TORQUE FROM CHANGING DRILL TRAJECTORY WITH TIP OF DRILL STILL IN THE BONE."

  Patient problems: Foreign Body In Patient

  MAUDE report 23646557 ↗