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Tools - WFS IMPCT-WHDRecalls & reported problems

Trimed, INC. · Wrist Hook Dorsal Impactor · Class 1

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00842188113659), received between Apr 11, 2018 and May 16, 2018 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Corroded” (2 reports).

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

  • Corroded2

Patient problems

  • No Patient Involvement2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 16, 2018Corroded

    ON (B)(6) 2018, (B)(6) REPORTED THAT A WRIST HOOK DORSAL IMPACTOR (IMPCT-WHD) WAS FOUND TO HAVE SHOWN SIGNS OF RUST ON THE HANDLE. THE NONCONFORMING PART WAS FOUND DURING A TRAY REPLACEMENT INSPECTION AND HAD NO CONTACT WITH A PATIENT. THIS IS THE FOURTH TIME THAT THIS TYPE OF MALFUNCTION HAS OCCURRED FOR THIS PART.

    Patient problems: No Patient Involvement

    MAUDE report 7520554 ↗
  • MalfunctionApr 11, 2018Corroded

    ON (B)(6) 2018, (B)(6) REPORTED THAT A WRIST HOOK DORSAL IMPACTOR (IMPCT-WHD) WAS FOUND TO HAVE SHOWN SIGNS OF RUST ON THE HANDLE. THE NONCONFORMING PART WAS FOUND DURING A TRAY REPLACEMENT INSPECTION AND HAD NO CONTACT WITH A PATIENT. THIS IS THE THIRD TIME THAT THIS TYPE OF MALFUNCTION HAS OCCURRED FOR THIS PART.

    Patient problems: No Patient Involvement

    MAUDE report 7423902 ↗

Other IMPACTOR devices

All IMPACTOR devices →

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