Acetaminophen Regular Strength recall: Labeling Error
Acetaminophen Regular Strength, 325 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC…
Why was Acetaminophen Regular Strength recalled?
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: KDT0124001, Exp 08/31/2026
- Product
- Acetaminophen Regular Strength, 325 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC…
- Recalling firm
- Akron Pharma, Inc.
- Quantity
- 6429 bottles
- Distribution
- Nationwide in the US
- Recall date
- January 22, 2025
- Classification
- Class III
- Status
- Ongoing
- Agency
- FDA (drug)