FDAFDA · Food and drugs·Recall number Z-2883-2018
GENESIS II NON-POROUS CRUCIATE RETAINING FEMORAL COMPONENT, SIZE 6 RIGHT, REF 71420026 Knee prosthesis
Published August 29, 2018 · Recall initiated: August 1, 2017
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
Two lots of Genesis II Non Porous C/R Femoral Size 6 right packaged were distributed containing Genesis II C/R Femoral Size 4 left.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Smith & Nephew, Inc.
- Distributor
- Australia, Austria, Germany, Great Britain, Poland, Spain
- Lot
- Lot Numbers: 16CMB0061A, 16CMB0066A
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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