Femhrt (norethindrone recalls
The FDA has published 2 recalls involving Femhrt (norethindrone since 2013. The latest was reported on 8 May 2013. Most were for packaging defects. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls2since 2013
Last 12 months0reported
Class I00% of total
Ongoing0latest 8 May 2013
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 0 0%Class III 2 100%
Why femhrt (norethindrone is recalled
Companies
By year
All femhrt (norethindrone recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Femhrt (norethindrone acetate recalled by Warner Chilcott Company | Warner Chilcott | Packaging Defects | Nationwide |
| Drug | CLASS III | Femhrt (norethindrone acetate recalled by Warner Chilcott Company | Warner Chilcott | Packaging Defects | Nationwide |
Should you stop taking Femhrt (norethindrone?
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.