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device recall
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BioPro, Inc. device recall (Cls II)

September 9, 2025updated 5mo ago
community read0 votes

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 — Reason: 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. — Status: Ongoing

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same company · ±60 days · 6

  • device recallBioPro, Inc. device recall (Cls II)Sep 9, 2025
  • device recallBioPro, Inc. device recall (Cls II)Sep 9, 2025
  • device recallBioPro, Inc. device recall (Cls II)Sep 9, 2025
  • device recallBioPro, Inc. device recall (Cls II)Sep 9, 2025
  • device recallBioPro, Inc. device recall (Cls II)Sep 9, 2025
  • approvalMIFEPRISTONE: MIFEPRISTONE — FDA approvalSep 30, 2025

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