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FDAAugust 5, 2015device

Biomet Parsippany, NJ. 4 0 MM X 14 MM Variable Screw C-Tek Maxan Anterior Cervical Plate System. Lot 375440.

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

The hazard

Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.

What to do

FDA enforcement status: Terminated

Brands named

biomet spinebiomet

Recall history

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

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