Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., 373 US RT 46 W Building E, Suite 117, Fairfield, NJ 07034, NDC 71399-8022-02
Reported: January 22, 2025 Initiated: December 12, 2024 #D-0196-2025
Product Description
Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., 373 US RT 46 W Building E, Suite 117, Fairfield, NJ 07034, NDC 71399-8022-02
Reason for Recall
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Details
- Recalling Firm
- Akron Pharma, Inc.
- Units Affected
- 1232 bottles
- Distribution
- Nationwide in the US
- Location
- Fairfield, NJ
Frequently Asked Questions
What product was recalled? ▼
Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., 373 US RT 46 W Building E, Suite 117, Fairfield, NJ 07034, NDC 71399-8022-02. Recalled by Akron Pharma, Inc.. Units affected: 1232 bottles.
Why was this product recalled? ▼
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 22, 2025. Severity: Low. Recall number: D-0196-2025.
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