Stanmore Implants Worldwide Ltd. recalls Femoral Shaft L=120mm; Femoral Shaft L=135mm; Femoral Shaft L=150mm The product is a component is a systems that is int…

Recall date

December 7, 2016

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0822-2017

FDA classification

Class II

Brand / firm

Stanmore Implants Worldwide Ltd.

Sold / distributed

Nationwide Distribution to OH, NE, FL, LA, NY, TX, MS, MD, CT, AL, PA

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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