Klassic Blade Offset Femoral Stem, Porous, Size 6 3107.06.000Recalls & reported problems
Total Joint Orthopedics, Inc. · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00814703012341), received between Feb 25, 2026 and Feb 25, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Implant subsidence” (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.
Reports received per month
Most reported problems
Device problems
- Implant subsidence1
Patient problems
- Bone Fracture(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 25, 2026Implant subsidence
A SERIOUS INJURY RESULTED IN THE NEED FOR SURGICAL INTERVENTION DUE TO A SPONTANEOUS VANCOUVER TYPE B2 FRACTURE WITH STEM SUBSIDENCE 10 DAYS AFTER THE PRIMARY THA SURGERY WITH NO REPORTED FALL OR INCIDENT BY THE PATIENT. SURGEON REPORTED THE PATIENT WAS VERY OSTEOPOROTIC WITH A TYPE C FEMUR.
Patient problems: Bone Fracture(s)
MAUDE report 24449125 ↗
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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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