Angiodynamics Inc. (Navilyst Medical Inc.) recalls RS 5F DL BIOFLO PASV, Catalog Number 60M183481
Recalled Product
RS 5F DL BIOFLO PASV, Catalog Number 60M183481
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: H96560M1834811; Lot: 5301023, 5310193, 5312020
View official government recall
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