Cook Biotech Incorporated
20 devices · 18 adverse event reports · 2 deaths reported · 8 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- Biodesign G31455Mesh, surgical, collagen, diaphragmatic hernia1 recall1 report
- Biodesign G31091DURA SUBSTITUTE1 recall0 reports
- Biodesign G54612Mesh, surgical1 recall0 reports
- Biodesign G54613Mesh, surgical1 recall0 reports
- Biodesign G54614Mesh, surgical1 recall0 reports
- Biodesign G60285POLYMER, ENT SYNTHETIC-POLYAMIDE (MESH OR FOIL MATERIAL)1 recall0 reports
- Biodesign G31091DURA SUBSTITUTE1 recall0 reports
- Biodesign G31141Mesh, surgical1 recall0 reports
- Biodesign G46600Mesh, surgical, collagen, large abdominal wall defects1 death3 reports
- Biodesign G36032Mesh, surgical, collagen, large abdominal wall defects1 death2 reports
- BIODESIGN G44451POLYMER, ENT SYNTHETIC-POLYAMIDE (MESH OR FOIL MATERIAL)2 reports
- Biodesign G48216Mesh, surgical, collagen, large abdominal wall defects2 reports
- Biodesign G23653Mesh, surgical1 report
- Biodesign G36033Mesh, surgical, collagen, large abdominal wall defects1 report
- Biodesign G44839POLYMER, ENT SYNTHETIC-POLYAMIDE (MESH OR FOIL MATERIAL)1 report
- Zenapro G23770Mesh, surgical, polymeric1 report
- Biodesign G31090DURA SUBSTITUTE1 report
- Biodesign G31092DURA SUBSTITUTE1 report
- Biodesign G34979DURA SUBSTITUTE1 report
- Zenapro G35477Mesh, surgical, polymeric1 report