Severity
Critical
CriticalClass ITerminated
FDA Drug recall · Reported August 14, 2024
Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles, Packaged By: A-S Medication Solutions, Libertyville, IL 60048. NDC: 50090-5313-2
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.
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
A-s Medication Solutions LLC recalled Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles, Packaged By: A-S Me… - a critical-severity action.
Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles, Packaged By: A-S Me… was recalled by A-s Medication Solutions LLC in August 14, 2024. Reason: Labeling: Label Mix-Up: Some bottles of Acetaminophen Extra Strength 500 mg tablets were incorrectly labeled …. Check the official notice for the remedy. Verify recall #D-0631-2024 with the FDA Drug before acting.
The recall
A-s Medication Solutions LLC issued this critical-severity FDA Drug recall-Labeling: Label Mix-Up: Some bottles of Acetaminophen Extra Strength 500 mg tablets were incorrectly labeled ….
- Critical
- severity level
- Class I
- classification
- August 14, 2024
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0631-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0631-2024) was formally reported on August 14, 2024, with the manufacturer initiating the action on June 21, 2024. It is classified under Critical severity (Class I), with a current status of Terminated. A-s Medication Solutions LLC is listed as the recalling firm, operating out of Libertyville, IL. Federal records list the affected scope as 429 bottles.
The documented reason for this recall is: 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. Distribution data in the federal record shows the product reached: Nationwide within the United States.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 5 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
429 bottles
Related Recalls
6
5 from same agency
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | D-0631-2024 |
| Date reported | August 14, 2024 |
| Date initiated | June 21, 2024 |
| Recalling firm | A-s Medication Solutions LLC |
| Firm location | Libertyville, IL |
| Affected scope | 429 bottles |
| Distribution | Nationwide within the United States. |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0631-2024) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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.
Where was the recalled product distributed? ▼
Distribution: Nationwide within the United States..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0631-2024) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported August 14, 2024. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.