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FDASeptember 15, 2017device

36MM COCR MODULAR HD -6MM

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

The hazard

One piece from a different lot mixed with lot 236840 and is incorrectly etched as -6MM offset instead of +3MM offset. As the incorrect etching and related size difference affects the functional use of this product, the affected lot is being removed from the field.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

UPCs

00880304210509

Recall history

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

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