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Tornier Perform MWE114Recalls & reported problems

Tornier · Glenoid Grasper · 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 03700386973598), received between Nov 27, 2020 and Nov 27, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Failure to Clean Adequately” (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

  • Failure to Clean Adequately1
  • Residue After Decontamination1

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.

  • InjuryNov 27, 2020Residue After Decontamination; Failure to Clean Adequately; Residue After Decontamination; Failure to Clean Adequately

    THE GLENOID GRASPER HAD CEMENT ON THE PART THAT HOLDS THE IMPLANT. SURGERY CONTINUED AND THE SURGEON DID NOT USE THE INSTRUMENT. NO BACKUP SET WAS AVAILABLE. SURGEON INSERTED THE IMPLANT MANUALLY TO THE GLENOID. AT THE END OF THE CASE SURGEON DOUBLED THE ANTIBIOTIC DOSE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 10913705 ↗

Other FORCEPS devices

All FORCEPS devices →

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