# FDA recall D-0210-2018

> **Woodfield Pharmaceutical, LLC** · Class II · drug recall initiated 2017-12-12.

## Product

Codeine-Guaifenesin Oral Solution 10-100 mg/5 mL Antitussive Expectorant ,16 fl. oz. , Manufactured For: Method Pharmaceuticals, LLC Arlington, TX 76006, NDC 58657-500-16

## Reason for recall

Microbial Contamination of Non-Sterile Products: potentially contamination with the bacteria Burkholderia cepacia

## Distribution

Texas

## Key facts

- **Recall number:** D-0210-2018
- **Recalling firm:** Woodfield Pharmaceutical, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-12-12
- **Report date:** 2018-01-17
- **Termination date:** 2020-01-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Houston, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0210-2018

## Citation

> AI Analytics. FDA recall D-0210-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0210-2018. Source: US FDA. Licensed CC0.

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