Acetaminophen Extra Strength Per recalls
The FDA has published 2 recalls involving Acetaminophen Extra Strength Per since 2025. The latest was reported on 22 Jan 2025. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls2since 2025
Last 12 months0reported
Class I00% of total
Ongoing2latest 22 Jan 2025
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 acetaminophen extra strength per is recalled
Companies
By year
Ongoing acetaminophen extra strength per recalls
2 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Acetaminophen Extra Strength 500 mg per, Akron Pharma recalled | Akron Pharma | Other | Nationwide |
| Drug | CLASS III | Acetaminophen Extra Strength 500 mg per, Akron Pharma, Inc. recalled | Akron Pharma | Other | Nationwide |
All acetaminophen extra strength per recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Acetaminophen Extra Strength 500 mg per, Akron Pharma recalled | Akron Pharma | Other | Nationwide |
| Drug | CLASS III | Acetaminophen Extra Strength 500 mg per, Akron Pharma, Inc. recalled | Akron Pharma | Other | Nationwide |
Should you stop taking Acetaminophen Extra Strength Per?
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.