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PressFT TD21HRecalls & reported problems

Conmed Corporation · PressFT™ Drill Bit 2.1mm, Hip · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854901908), received between May 26, 2023 and May 26, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Material Fragmentation” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Material Fragmentation1

Patient problems

  • Foreign Body In Patient1

Recent adverse event reports

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

  • InjuryMay 26, 2023Material Fragmentation; Material Fragmentation

    INTERNATIONAL COMPLAINTS REPORTED ON BEHALF OF THE CUSTOMER THAT THE TD21H, PRESSFT DRILL BIT 2.1MM, HIP DEVICE WAS BEING USED DURING A HIP ARTHROSCOPY PROCEDURE ON (B)(6) 2023 WHEN IT WAS REPORTED ¿THE THIRD USE OF THE DRILL FOR THE INSERTION OF ACETABULAR IMPLANTS OCCURRED THE RUPTURE. THE PIECE IS TOTALLY INSIDE THE BONE WITHOUT SURFACING.¿. IT WAS ALSO REPORTED THAT ¿THE BROKEN DRILL BIT REMAINED IN THE PATIENT AND WAS NOT REMOVED.¿. THERE WAS NO REPORT OF SURGICAL INTERVENTION OR EXTENDED HOSPITALIZATION REQUIRED FOR THE PATIENT. THIS REPORT IS BEING RAISED ON THE REPORTED INJURY DUE TO FOREIGN BODY LEFT INSIDE THE PATIENT.

    Patient problems: Foreign Body In Patient

    MAUDE report 17010300 ↗

Other BIT, SURGICAL devices

All BIT, SURGICAL devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.