Reported Oct 22, 2025 · Ongoing

BioPro Bipolar Head Product ID/Description 18130 BIPOLAR HEAD 38MM 18131 BIPOLAR HEAD 39MM 18132 BIPOLAR HEAD 40MM…

BioPro, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: BioPro, Inc. · 2929 Lapeer Rd · Port Huron, MI · 48060-2558

Is this the product you have?

  • 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
Lot codes and dates
  • Product ID/UDI-DI
    • 18130
    • M20918130
    • 18131
    • M20918131
    • 18132
    • M20918132
    • 18133
    • M20918133
    • 18134
    • M20918134
    • 18135
    • M20918135
    • 18136
    • M20918136
    • 18137
    • M20918137
    • 18138
    • M20918138
    • 18139
    • M20918139
    • 18140
    • M20918140
    • 18141
    • M20918141
    • 18142
    • M20918142
    • 18143
    • M20918143
    • 18144
    • M20918144
    • 18145
    • M20918145
    • 18146
    • M20918146
    • 18147
    • M20918147
    • 18148
    • M20918148
    • 18149
    • M20918149
    • 18150
    • M20918150
    • 18151
    • M20918151
    • 18152
    • M20918152
    All lots, all serial numbers
Amount recalled
147 total

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Where it was sold

Why it was 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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:32 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.