FDAJanuary 11, 2016device

Product 2 consists of all products product code LPH, and same usage: 801802202 12/14 COCR FEMORAL HEAD 2 801802220 12/14 COCR FEMORAL HEAD 2 801802230 12/14 COCR FEMORAL HEAD 2 801802601 12/14 COCR FEMORAL HEAD 2 801802602 12/14 COCR FEMORAL HEAD 2 801802603 12/14 COCR FEMORAL HEAD 2 801802604 12...

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

80180220212280180222012280180223012280180260112280180260212280180260312280180260412280180260512280180280112280180280212280180280312280180280512

Recall history

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

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