FDASeptember 9, 2025device

BioPro Femoral Head Product ID/Description 14089 HEAD FEMORAL 28 SH LT 14090 HEAD FEMORAL 28 MD LT 14091 HEAD FEMORAL 28 LG LT 14094 HEAD FEMORAL 32 SH LT 14095 HEAD FEMORAL 32 MD LT 14096 HEAD FEMORAL 32 LG LT

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

The hazard

Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.

What to do

FDA enforcement status: Ongoing

Brands named

biopro

Recall history

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

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