← FDA ENFORCEMENT
D-0631-2024Class I

A-S Medication Solutions LLC

Recalling firm
A-S Medication Solutions LLC
Product type
Drug
Status
Terminated
Report date
2024-08-14
Distribution
Nationwide within the United States.
Firm state
IL
Product quantity
429 bottles
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Documentation & Change Control
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.

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

Code / lot info

Lot: 4138197; Exp 10/31/2025

Other recalls SPEQ maps to Documentation & Change Control
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See all Documentation & Change Control recalls →

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.