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Zimmer Manufacturing B.V. recalls Product 64 consists of all product under product code: JDI and same usage: Item no: 902605101 UNIPOLAR ENDO FEM HEAD

Recalled March 23, 2016 · FDA recall Z-1162-2016 · Zimmer Manufacturing B.V

Hazard
As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile. · FDA Class II
Units
0
Sold at
US Nationwide Distribution

Description

As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.

Product
Product 64 consists of all product under product code: JDI and same usage: Item no: 902605101 UNIPOLAR ENDO FEM HEAD 51MM For use in hemi hip arthroplasty
Manufacturer(s)
Zimmer Manufacturing B.V.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Zimmer Manufacturing B.V. recalls Product 64 consists of all product under product code: JDI and same usage: Item no: 902605101 UNIPOLAR ENDO FEM HEAD | RecallWatchUSA