FDAApril 16, 2015device

Mallory/Head Primary Hip System; Size 11, 160 mm, Lateralized Femoral Stem; Ti-6Al-4V; Porous Plasma Uncemented, & Mallory/Head Total Hip System Size 12, 165 mm, Bi- Metric Femoral Components. Hip joint replacement components include: femoral stems, femoral heads, acetabular shells, and acetabula...

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

The hazard

Biomet hip joint, knee joint and shoulder joint replacement components device labeling contains incorrect GTIN (Global Trade Identification Number) codes.

What to do

FDA enforcement status: Terminated

Brands named

biomet

Recall history

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

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