Recall: A-S Acetaminophen Labeled as Aspirin
A-S Medication Solutions recalls 429 bottles of Acetaminophen Extra Strength because they were incorrectly labeled with the drug facts for Aspirin 81 mg.
Stop using this now
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.
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What happened, in plain English
A-S Medication Solutions LLC is recalling a small batch of Acetaminophen Extra Strength Tablets (500 mg) because some bottles were mislabeled. The affected bottles carry the Drug Facts label for Aspirin 81 mg instead of Acetaminophen. This mix-up poses a risk to consumers who may take the medication without realizing they are ingesting aspirin, which can be dangerous for those with allergies or bleeding disorders. Read more at govinfonow.com/recall/32617-recall-a-s-acetaminophen-labeled-as-aspirin.
Source Summary by GovInfoNow · govinfonow.com/recall/32617-recall-a-s-acetaminophen-labeled-as-aspirin · Updated October 9, 2026 · FDA enforcement record: FDA #D-0631-2024
Cite this page
“Recall: A-S Acetaminophen Labeled as Aspirin.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/32617-recall-a-s-acetaminophen-labeled-as-aspirin. Based on FDA recall #D-0631-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0631-2024%22&limit=1).
Why it’s dangerous
The hazard is a labeling error where the Drug Facts panel for Aspirin 81 mg was placed on bottles containing Acetaminophen 500 mg. This creates a serious safety issue because users might assume the bottle contains aspirin when it does not, or vice versa, leading to potential allergic reactions, drug interactions, or incorrect dosing for pain and fever relief.
Who’s affected
Consumers who purchased the specific lot of Acetaminophen Extra Strength Tablets from A-S Medication Solutions. Individuals with aspirin allergies, bleeding risks, or those who cannot take NSAIDs are at highest risk if they unknowingly consume the mislabeled product.
How to tell if you have this one
Check your bottle for the following details: Brand/Packer: A-S Medication Solutions, Libertyville, IL 60048. Product: Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles. NDC: 50090-5313-2. Lot Number: 4138197. Expiration Date: 10/31/2025.
- Brand
A-S Medication Solutions- Category
Drug
What to do — step by step
Stop using the product
Do not consume the tablets if your bottle matches the recalled lot number and NDC listed in the recall notice.
Check the label details
Verify that your bottle has NDC 50090-5313-2, Lot 4138197, and an expiration date of 10/31/2025.
Contact the manufacturer
Reach out to A-S Medication Solutions for further instructions on disposal or return since no specific remedy is currently listed in the record.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide within the United States.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 11 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
How many bottles are being recalled?
A total of 429 bottles are included in this recall.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0631-2024 (June 21, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0631-2024 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.