Acetaminophen Extra Strength 500 mg recall: Labeling Error
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…
Why was Acetaminophen Extra Strength 500 mg 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 #s: KDT0224001B, Exp 08/31/2026; KDT0224002B, Exp 09/30/2026.
- Product
- 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…
- Recalling firm
- Akron Pharma, Inc.
- Quantity
- 1232 bottles
- Distribution
- Nationwide in the US
- Recall date
- January 22, 2025
- Classification
- Class III
- Status
- Ongoing
- Agency
- FDA (drug)