Recalls / —
—#25701
Product
Versys Hip System femoral stem, fiber metal midcoat, collared, 12/14 neck taper, low head center, size 14, standard body. Cat. No. 7841-14-10.
- FDA product code
- LPH — Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
- Device class
- Class 2
- Medical specialty
- Orthopedic
- 510(k) numbers
- K922071
- Affected lot / code info
- All lots.
Why it was recalled
The femoral heads will not seat onto the taper of the hip stem, as the head impinges on the radius undercut below the taper.
Root cause (FDA determination)
Other
Action the firm took
Recall letters dated 1/7/03 were sent to each U.S. consignee via certified mail, requesting that they contact Zimmer for pick-up of the products if any was in stock. Ex-U.S. consignees were notified via e-mail.
Recalling firm
- Firm
- Zimmer Inc.
- Address
- 345 E. Main St., Warsaw, Indiana 46580
Distribution
- Distribution pattern
- United States, Australia and Canada.
Timeline
- Recall initiated
- 2003-01-07
- Posted by FDA
- 2003-01-28
- Terminated
- 2004-02-09
- Status
- —
Source: openFDA Device Recall endpoint. Recall record ID #25701. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.