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RECAP/MAGNUM INSTRUMENTATION 31-158946Recalls & reported problems

Biomet Uk Ltd · 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 05019279120567), received between Aug 2, 2022 and Aug 2, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Positioning Failure” (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

  • Positioning Failure1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionAug 2, 2022Positioning Failure; Positioning Failure

    IT WAS REPORTED THAT THE CUP INSERTER WOULD NOT ASSEMBLE WITH THE CUP, LEADING THE SURGEON TO PLACE THE CUP BY SIMPLY HOLDING IT TO THE ACETABULUM. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15151009 ↗

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Sources and updates

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