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NA SD357.135Recalls & reported problems

Synthes GmbH · NAIL EXTRACTION SCREW CANNULATED · 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 10886982263063), received between Sep 29, 2023 and Sep 29, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device-Device Incompatibility” (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

  • Device-Device Incompatibility1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • MalfunctionSep 29, 2023Device-Device Incompatibility; Device-Device Incompatibility

    IT WAS REPORTED THAT ON AN UNKNOWN DATE IN 2023, THE EXTRACTION BOLT BECAME STUCK TO THE NAIL. NO ADDITIONAL INFORMATION IS AVAILABLE. THIS REPORT IS FOR A NAIL EXTRACTION SCREW CANNULATED. THIS IS REPORT 1 OF 2 FOR (B)(4).

    Patient problems: Insufficient Information

    MAUDE report 17842850 ↗

Other EXTRACTOR devices

All EXTRACTOR devices →

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