# FDA recall D-136-2013

> **Belmora LLC** · Class III · drug recall initiated 2012-12-18.

## Product

Flanax (aluminum hydroxide, magnesium hydroxide, and simethicone) Fast Acting Antacid, 200 mg/200 mg/20 mg, 12 fl oz (355 mL) bottles, Distributed by: Belmora LLC, PO Box 3063, Arlington, VA 22203, UPC 8 53030 00209 0, NDC 27854.101.01.

## Reason for recall

Defective Container: Product lacks tamper evident breakaway band on cap.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-136-2013
- **Recalling firm:** Belmora LLC
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-12-18
- **Report date:** 2013-01-30
- **Termination date:** 2013-04-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Arlington, VA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-136-2013

## Citation

> AI Analytics. FDA recall D-136-2013. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/D-136-2013. Source: US FDA. Licensed CC0.

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