Tools - WFS WHD-IMPACTRRecalls & reported problems
Trimed, INC. · Wrist Hook Dorsal Impactor · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00842188113666), received between Dec 14, 2017 and Dec 14, 2017 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Device Contamination with Chemical or Other Material1
- Material Erosion1
- Out-Of-Box Failure1
Patient problems
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 14, 2017Out-Of-Box Failure; Device Contamination with Chemical or Other Material
ON (B)(4) 2017 A SALES REP REPORTED THAT TWO WRIST HOOK DORSAL IMPACTOR (IMPCT-WHD) WERE FOUND WITH RUST ON THE GRIP HANDLE. THE NONCONFORMING PARTS WERE FOUND UPON OPENING THE WRIST HOOK SET IN THE CLINICAL SETTING. THE IMPCT-WHD IS ENCLOSED IN THE WRIST HOOK SET, THE NONCONFORMING PART WAS VISIBLE UPON OPENING OF THE SET AND WAS NEVER REMOVED OUR TOUCHED, AND THE SET WAS IMMEDIATELY CLOSED BACK UP. THE ENTIRE SET WAS IMMEDIATELY REPLACED WITH AN ENTIRELY NEW SET OF PARTS AND TOOLS WERE USED, NO ADVERSE EVENTS WERE REPORTED. THIS IS THE FIRST TIME THAT THIS TYPE OF MALFUNCTION HAS OCCURRED FOR THIS PART.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7119454 ↗MalfunctionDec 14, 2017Material Erosion
ON (B)(6) 2017 A SALES REP REPORTED THAT TWO WRIST HOOK DORSAL IMPACTOR (IMPCT-WHD) WERE FOUND WITH RUST ON THE GRIP HANDLE. THE NONCONFORMING PARTS WERE FOUND UPON OPENING THE WRIST HOOK SET IN THE CLINICAL SETTING. THE IMPCT-WHD IS ENCLOSED IN THE WRIST HOOK SET, THE NONCONFORMING PART WAS VISIBLE UPON OPENING OF THE SET AND WAS NEVER REMOVED OUR TOUCHED, AND THE SET WAS IMMEDIATELY CLOSED BACK UP. THE ENTIRE SET WAS IMMEDIATELY REPLACED WITH AN ENTIRELY NEW SET OF PARTS AND TOOLS WERE USED, NO ADVERSE EVENTS WERE REPORTED. THIS IS THE FIRST TIME THAT THIS TYPE OF MALFUNCTION HAS OCCURRED FOR THIS PART.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7119452 ↗
Other IMPACTOR devices
- PINNACLE 2217-50-041Depuy (Ireland) · IMPACTOR4,295 reports
- ATTUNE 2544-01-006Depuy (Ireland) · IMPACTOR1 recall2,539 reports
- ATTUNE 2544-01-003Depuy (Ireland) · IMPACTOR1 recall1,498 reports
- ATTUNE 2544-01-017Depuy (Ireland) · IMPACTOR1 recall1,456 reports
- ATTUNE 2544-01-004Depuy (Ireland) · IMPACTOR1 recall875 reports
- DURALOC 2360-71-000Depuy Orthopaedics, Inc. · IMPACTOR716 reports
- SPECIALIST 2581-11-000Depuy (Ireland) · IMPACTOR704 reports
- INHANCE 6205-10-103Depuy (Ireland) · IMPACTOR337 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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