Recall
FDAHealthSeptember 9, 2025

BioPro, Inc. — 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

⚠️ 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.

Is this relevant to me?

Geography
US
Source agency
FDA
Category
Health
Published
September 9, 2025

US Domestic distribution to Texas and Michigan.

What's affected?

Product
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
Lot code
s

Additional details

Product ID/UDI-DI 14089 M20914089 14090 M20914090 14091 M20914091 14094 M20914094 14095 M20914095 14096 M20914096 All lots, all serial numbers

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 147 total.

View original FDA notice →

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