Recalls / Active ingredient / Iohexol
Iohexol
1 FDA drug recall involving the active ingredient “Iohexol”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2018-10-29 | Class II | Omnipaque (iohexol) Injection, 180mgI/mL, 20 mL Single-Dose Vial, packaged in 10 x 20 mL Vials per carton, Rx | GE Healthcare Inc. Life Sciences |