# FDA recall D-850-2013

> **GlaxoSmithKline, LLC.** · Class III · drug recall initiated 2013-07-18.

## Product

TUMS, Antacid/Calcium Supplement, ULTRA Strength 1000, Assorted Berries, 72 Chewable Tablets, GlaxoSmithKline, Moon Twp, PA 15108,  NDC 0135-0181-02

## Reason for recall

Presence of Foreign Tablets/Capsules: Product labeled TUMS Ultra Assorted Berries 1000mg Chewable tables, may contain EX TUMS Assorted Berries 750mg tablets

## Distribution

U.S. Nationwide

## Key facts

- **Recall number:** D-850-2013
- **Recalling firm:** GlaxoSmithKline, LLC.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-07-18
- **Report date:** 2013-08-14
- **Termination date:** 2016-05-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Zebulon, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-850-2013

## Citation

> AI Analytics. FDA recall D-850-2013. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/D-850-2013. Source: US FDA. Licensed CC0.

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