# FDA recall D-0631-2024

> **A-S Medication Solutions LLC** · Class I · drug recall initiated 2024-06-21.

## Product

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.

## Distribution

Nationwide within the United States.

## Key facts

- **Recall number:** D-0631-2024
- **Recalling firm:** A-S Medication Solutions LLC
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2024-06-21
- **Report date:** 2024-08-14
- **Termination date:** 2025-05-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Libertyville, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0631-2024

## Citation

> AI Analytics. FDA recall D-0631-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-0631-2024. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
