DJO SURGICAL 800-06-009Recalls & reported problems
Encore Medical, L.P. · INS, KNEE, EMPOWR, Femoral Impactor · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00190446317845), received between Dec 17, 2021 and Dec 17, 2021 — 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Break1
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.
MalfunctionDec 17, 2021Break
INSTRUMENT FAILURE - DURING INSPECTION OF EMPOWR UNI, FOUND 1 FEMORAL IMPACTOR HEAD WAS LOOSE ON HANDLE AND IT BROKE OFF IN MY HAND. HAD IT BEEN USED IN A SURGERY IT WOULD HAVE BROKE OFF ON IMPACT. WHILE INSPECTING ANOTHER FEMORAL IMPACTOR SURGEON FOUND THE SAME ISSUE. AND HAVE NOTICED THAT THESE AFTER A FEW USES ARE VERY DELICATE AND COULD BE LOOSE OR BROKEN. THIS MAY CAUSE AN ISSUE IF IT BREAKS DURING PROCEDURE WITH NO BACK UP. IMPACTION IS THE CAUSE OF INSTRUMENT FAILURE WHICH IS THE INSTRUMENTS INTENDED USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13030228 ↗
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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