Angiodynamics Inc. (Navilyst Medical Inc.) recalls BioFlo Midline 5F DL-20cm Max Sterile Barrier Drape Kit w/ T
Recalled Product
BioFlo Midline 5F DL-20cm Max Sterile Barrier Drape Kit w/ Two Nitinol Guidewire PG, Catalog Number 46-490
Hazard / Issue
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Issued by
FDA
Affected States: AZ, CA, CO, CT, DC, FL, GA, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, MT, NC, ND, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, WA, WI, WV
Lot/Code Info: UPN: H965464901; Lot: 5302405, 5312036, 5314940
View official government recall
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