African Black Ant recalls
The FDA has published 2 recalls involving African Black Ant since 2014. The latest was reported on 8 Oct 2014. Most were for labeling errors. Eugene Oregon 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 2014
Last 12 months0reported
Class I2100% of total
Ongoing0latest 8 Oct 2014
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 2 100%Class II 0 0%Class III 0 0%
Why african black ant is recalled
Companies
By year
All african black ant recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | African Black Ant, 2800 mg recalled by Eugene Oregon | Eugene Oregon | Labeling Errors | 11 states |
| Drug | CLASS I | African Black Ant, 2800 mg recalled by Nova Products | Nova Products | Labeling Errors | Nationwide |
Should you stop taking African Black Ant?
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.