FDAFDA · Food and drugs·Recall number Z-1704-2018
ATTUNE Revision CRS Femoral RT SZ 5 Cemented, Catalog No. 150440205, Femoral Revision Implant, Knee
Published May 16, 2018 · Recall initiated: April 16, 2018
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
There may be burrs on the extraction hole threads.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- DePuy Orthopaedics, Inc.
- Distributor
- The products were distributed to the following US states: FL, MO, and PA.
- Lot
- Lot Number HD6516, GTIN Number 10603295042280
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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