PlainRecalls
FDA Drug Critical Class I Terminated

Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles, Packaged By: A-S Medication Solutions, Libertyville, IL 60048. NDC: 50090-5313-2

Reported: August 14, 2024 Initiated: June 21, 2024 #D-0631-2024

Product Description

Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles, Packaged By: A-S Medication Solutions, Libertyville, IL 60048. NDC: 50090-5313-2

Reason for Recall

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.

Details

Units Affected
429 bottles
Distribution
Nationwide within the United States.
Location
Libertyville, IL

Frequently Asked Questions

What product was recalled?
Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles, Packaged By: A-S Medication Solutions, Libertyville, IL 60048. NDC: 50090-5313-2. Recalled by A-S Medication Solutions LLC. Units affected: 429 bottles.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Drug on August 14, 2024. Severity: Critical. Recall number: D-0631-2024.