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NA 387.293Recalls & reported problems

Synthes GmbH · UNIVERSAL PLATE BENDER · 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 10705034771021), received between Oct 18, 2018 and Oct 18, 2018 — 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Break1

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.

  • MalfunctionOct 18, 2018Break; Break

    THIS WAS DISCOVERED PRIOR TO THE OPERATION WHICH WAS CARRIED OUT AND COMPLETED SUCCESSFULLY WITH NO DELAYS. THE PATIENT WAS STABLE FOLLOWING THE PROCEDURE

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7980199 ↗

Other BENDER devices

All BENDER devices →

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