GENESIS II NON-POROUS CRUCIATE RETAINING FEMORAL COMPONENT, SIZE 6 RIGHT, REF 71420026 Knee prosthesis
Reported: August 29, 2018 Initiated: August 1, 2017 #Z-2883-2018
Product Description
GENESIS II NON-POROUS CRUCIATE RETAINING FEMORAL COMPONENT, SIZE 6 RIGHT, REF 71420026 Knee prosthesis
Reason for Recall
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.
Details
- Recalling Firm
- Smith & Nephew, Inc.
- Units Affected
- 27 units
- Distribution
- Australia, Austria, Germany, Great Britain, Poland, Spain
- Location
- Memphis, TN
Frequently Asked Questions
What product was recalled? ▼
GENESIS II NON-POROUS CRUCIATE RETAINING FEMORAL COMPONENT, SIZE 6 RIGHT, REF 71420026 Knee prosthesis. Recalled by Smith & Nephew, Inc.. Units affected: 27 units.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 29, 2018. Severity: Moderate. Recall number: Z-2883-2018.
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