Angiodynamics Inc. (Navilyst Medical Inc.) Recall: 5F DL BIOFLO PASV, Catalog Number 60M14
Angiodynamics Inc. (Navilyst Medical Inc.) Recall: 5F DL BIOFLO PASV, Catalog Number 60M14 is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Angiodynamics Inc. (Navilyst Medical Inc.); Product: 5F DL BIOFLO PASV, Catalog Number 60M141006; Reason for recall: A component of the kits might
| Recalling firm | Angiodynamics Inc. (Navilyst Medical Inc.) |
|---|---|
| Product | 5F DL BIOFLO PASV, Catalog Number 60M141006 |
| Reason for recall | A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | The products were distributed to the following US 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, and WV. The products were distributed to the following foreign countries: Canada, China, Ireland, Spain. |
| Recall initiated | 20180510 |
| Recall number | Z-2207-2018 |
| Category | device |
| State | NY |
| Country | United States |
$29/mo
Try RecallGuard →