Iohexol Iodine recalls
The FDA has published 2 recalls involving Iohexol Iodine since 2012. The latest was reported on 21 Dec 2022. Most were for sterility. BayCare Integrated Service Center, LLC / has the most recalls in this group. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls2since 2012
Last 12 months0reported
Class I150% of total
Ongoing0latest 21 Dec 2022
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 1 50%Class II 1 50%Class III 0 0%
Why iohexol iodine is recalled
Companies
By year
All iohexol iodine recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Iohexol (300 mg Iodine/mL) Iodine/, Total Volume in syringe recalled | BayCare Integrated Service Center, LLC / | Labeling Errors | FL |
| Drug | CLASS II | Iohexol 200mg Iodine/ML Injectable recalled by Franck's Lab Inc., d.b.a. | Franck's Lab Inc., d.b.a. Franck's Compounding Lab | Sterility | Nationwide |
Should you stop taking Iohexol Iodine?
Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.