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Stanmore Implants Worldwide Ltd. recalls Distal Femoral Replacement (patient specific, custom made orthopedic implant device). PIN 19960
Recalled May 18, 2016 · FDA recall Z-1623-2016 · Stanmore Implants Worldwide
Hazard
Incorrect component used to manufacture distal femoral replacement. · FDA Class II
Units
1
Sold at
US distribution to OH.
Description
Incorrect component used to manufacture distal femoral replacement.
Product
Distal Femoral Replacement (patient specific, custom made orthopedic implant device). PIN 19960
Manufacturer(s)
Stanmore Implants Worldwide Ltd.
Made in
United Kingdom
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →