De-fibroidin recalls
The FDA has published 1 recall involving De-fibroidin since 2020. The latest was reported on 15 Apr 2020. Most were for labeling errors. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls1since 2020
Last 12 months0reported
Class I00% of total
Ongoing0latest 15 Apr 2020
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 1 100%Class III 0 0%
Why de-fibroidin is recalled
Companies
By year
All de-fibroidin recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | De-Fibroidin, 500mg Capsules recalled by Herbal Doctor Remedies | Herbal Doctor Remedies | Labeling Errors | CA |
Should you stop taking De-fibroidin?
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.