Recalls / Active ingredient / Ioversol
Ioversol
1 FDA drug recall involving the active ingredient “Ioversol”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2019-09-13 | Class II | Optiray 320 (ioversol) Injection 68%, 320 mg/mL Organically Bound Iodine, packaged in 1 - 100 mL Ultraject Pre | GUERBET LLC |