Acetaminophen Extra Strength Tablets recall: Labeling Error
Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles, Packaged By: A-S Medication Solutions, Libertyville, IL 60048. NDC: 50090-5313-2
Why was Acetaminophen Extra Strength Tablets recalled?
Labeling: Label Mix-Up: Some bottles of Acetaminophen Extra Strength 500 mg tablets were incorrectly labeled with the drug facts label for Aspirin 81 mg tablets.
What should I do if I have this product?
Review the official FDA enforcement record for current 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: 4138197; Exp 10/31/2025
- Product
- Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles, Packaged By: A-S Medication Solutions, Libertyville, IL 60048. NDC: 50090-5313-2
- Recalling firm
- A-S Medication Solutions LLC
- Quantity
- 429 bottles
- Distribution
- Nationwide within the United States.
- Recall date
- August 14, 2024
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)