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NA 2544-00-100Recalls & reported problems

Depuy (Ireland) · PRIMARY CUTS AND SIZING PACK · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295129844), received between Oct 9, 2020 and Oct 9, 2020 — classified as 1 malfunction.

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

Device problems

  • Break1
  • Loose or Intermittent Connection1

Patient problems

  • No Code Available1
  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionOct 9, 2020Break; Loose or Intermittent Connection; Break; Loose or Intermittent Connection

    IT WAS REPORTED THAT THE SCREW AND WASHER CAME OUT OF THE RIGHT TIBIAL CUTTING GUIDE ON THE RIGHT SIDE. ALL PIECES WERE RETRIEVED FROM THE PATIENT AND THIS DID NOT DELAY SURGERY.

    Patient problems: No Code Available; No Consequences Or Impact To Patient

    MAUDE report 10656941 ↗

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Sources and updates

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