# FDA recall D-829-2013

> **Actavis South Atlantic LLC** · Class II · drug recall initiated 2013-05-15.

## Product

Ranitidine Syrup (Ranitidine Oral Solution USP) 15 mg/mL, Rx Only.  Manufactured by VistaPharm, Inc., Birmingham, AL 35242.  Distributed by Actavis Mid Atlantic LLC 1877 Kawai Road, Lincolnton, NC  28092 USA

## Reason for recall

Failed Impurity/Degradation Specification; "Related Compound C"

## Distribution

Nationwide

## Key facts

- **Recall number:** D-829-2013
- **Recalling firm:** Actavis South Atlantic LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-05-15
- **Report date:** 2013-08-07
- **Termination date:** 2014-05-15

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-829-2013

## Citation

> AI Analytics. FDA recall D-829-2013. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-829-2013. Source: US FDA. Licensed CC0.

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