# FDA recall D-0391-2022

> **Medique Products** · Class II · drug recall initiated 2021-12-06.

## Product

Extra Strength Headache (acetaminophen 250 mg, aspirin 250 mg, caffeine 65 mg) tablets, packaged in 2-count tablets per packet, Manufactured for: Lil' Drug Store Products, Inc., Cedar Rapids, IA 52404

## Reason for recall

CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0391-2022
- **Recalling firm:** Medique Products
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2021-12-06
- **Report date:** 2022-01-26
- **Termination date:** 2023-06-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Fort Myers, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0391-2022

## Citation

> AI Analytics. FDA recall D-0391-2022. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/D-0391-2022. Source: US FDA. Licensed CC0.

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