FDA-Device2016-12-28Class II
Femoral Shaft L=120mm; Femoral Shaft L=135mm; Femoral Shaft L=150mm The product is a component is a systems that is intended for the replacement if diseased or deficient bone around the knee joint, distal femur, proximal femur or total femur bone
Stanmore Implants Worldwide Ltd.
Hazard
The recalling firm has received 5 customer inquiries reporting that at least one pouch of the double pouch packaging configuration has been punctured by the tip of the device's stem.
Sold states
Nationwide Distribution to OH, NE, FL, LA, NY, TX, MS, MD, CT, AL, PA
Affected count
11 units
Manufactured in
210 Centennial Avenue Centennial Park, Centennial Park, Borehamwood, N/A, United Kingdom
Products
Femoral Shaft L=120mm; Femoral Shaft L=135mm; Femoral Shaft L=150mm The product is a component is a systems that is intended for the replacement if diseased or deficient bone around the knee joint, distal femur, proximal femur or total femur bone
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0822-2017Don't want to check this manually?
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