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LPS 2987-99-032Recalls & reported problems

Depuy (Ireland) · LPS PROX TIB & PROX FEM TRIAL INST · Class 1

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 10603295159575), received between Jul 10, 2020 and Jul 10, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Component Missing” (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

  • Component Missing1

Patient problems

  • 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.

  • MalfunctionJul 10, 2020Component Missing; Component Missing

    IT WAS REPORTED THAT THE RUBBER BUSHINGS THAT HOLD THE RULER HAVE FALLEN OUT AND ONE OF THE HANDLES ON THE OUTSIDE OF THE LPS INSTRUMENTATION PAN IS MISSING. HANDLE ALSO MISSING FROM THE PROXIMAL PAN. NO SURGICAL DELAY.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10257985 ↗

Other TRAY, SURGICAL, INSTRUMENT devices

All TRAY, SURGICAL, INSTRUMENT devices →

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