# FDA recall D-1287-2015

> **GlaxoSmithkline Consmer Healthcare** · Class III · drug recall initiated 2015-06-30.

## Product

Panadol (acetaminophen) Extra Strength, 500 mg, a) 30 count (UPC 1-03-53100-91070-8, NDC 0135-0135-02), b) 60 count (UPC 1-03-53100-91080-7, NDC 0135-0135-03) and c) 100 count (UPC 1-03-53100-91090-6, NDC 0135-0135-04) bottles, Distributed by: GlaxoSmithKline Consumer Healthcare L.P, Moon Township, PA 15108

## Reason for recall

Failed Dissolution Specifications

## Distribution

Puerto Rico and Virgin Islands

## Key facts

- **Recall number:** D-1287-2015
- **Recalling firm:** GlaxoSmithkline Consmer Healthcare
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-06-30
- **Report date:** 2015-08-12
- **Termination date:** 2017-02-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Moon Township, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1287-2015

## Citation

> AI Analytics. FDA recall D-1287-2015. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-1287-2015. Source: US FDA. Licensed CC0.

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