BioPro, Inc.: Device Recall
Recall #Z-0150-2026 · 09/09/2025
Recall Details
- Recall Number
- Z-0150-2026
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- BioPro, Inc.
- Status
- Ongoing
- Date Initiated
- 09/09/2025
- Location
- Port Huron, MI, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 147 total
Reason for Recall
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.
Product Description
BioPro Bipolar Head Product ID/Description 18130 BIPOLAR HEAD 38MM 18131 BIPOLAR HEAD 39MM 18132 BIPOLAR HEAD 40MM 18133 BIPOLAR HEAD 41MM 18134 BIPOLAR HEAD 42MM 18135 BIPOLAR HEAD 43MM 18136 BIPOLAR HEAD 44MM 18137 BIPOLAR HEAD 45MM 18138 BIPOLAR HEAD 46MM 18139 BIPOLAR HEAD 47MM 18140 BIPOLAR HEAD 48MM 18141 BIPOLAR HEAD 49MM 18142 BIPOLAR HEAD 50MM 18143 BIPOLAR HEAD 51MM 18144 BIPOLAR HEAD 52MM 18145 BIPOLAR HEAD 53MM 18146 BIPOLAR HEAD 54MM 18147 BIPOLAR HEAD 55MM 18148 BIPOLAR HEAD 56MM 18149 BIPOLAR HEAD 57MM 18150 BIPOLAR HEAD 58MM 18151 BIPOLAR HEAD 59MM 18152 BIPOLAR HEAD 60MM
Distribution Pattern
US Domestic distribution to Texas and Michigan.
Other Recalls by BioPro, Inc.
- Class II: Risk 09/09/2025
- Class II: Risk 09/09/2025
- Class II: Risk 09/09/2025
- Class II: Risk 09/09/2025
- Class II: Risk 09/09/2025