FDAJanuary 11, 2016device

Product 57 consists of all product code: JDI and same usage: Item no: 763401000 PRESSFIT FEM ST FX 10 X 115 763401100 PRESSFIT FEM ST FX 11 X 1 763401200 PRESSFIT FEM ST FX 12 X 1 763401300 PRESSFIT FEM ST FX 13 X 1 763401400 PRESSFIT FEM ST FX 14 X 1 763401500 PRESSFIT FEM ST FX 15 X 1 For use i...

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Terminated

Brands named

zimmer manufacturing b vzimmerzimmer manufacturing

UPCs

115763401100

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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