Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BioPro Femoral Head Product ID/Description 14089 HEAD FEMORAL 28 SH Recalled by BioPro, Inc. Due to Potential packaging issue that could compromise the sterile...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact BioPro, Inc. directly.
Affected Products
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
Quantity: 147 total
Why Was This Recalled?
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.
Where Was This Sold?
US Domestic distribution to Texas and Michigan.
About BioPro, Inc.
BioPro, Inc. has 37 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report