Excedrin Extra Strength (acetaminophen recalls
The FDA has published 1 recall involving Excedrin Extra Strength (acetaminophen since 2013. The latest was reported on 14 Aug 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 recalls1since 2013
Last 12 months0reported
Class I00% of total
Ongoing0latest 14 Aug 2013
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 excedrin extra strength (acetaminophen is recalled
Companies
By year
All excedrin extra strength (acetaminophen recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Excedrin Extra Strength (Acetaminophen 250 mg, Aspirin recalled | Novartis Consumer Health | Packaging Defects | Nationwide |
Should you stop taking Excedrin Extra Strength (acetaminophen?
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.