US Drug Recall Register
Class II · Moderate risk Terminated Initiated Dec 12, 2017 (9 years ago)

Codeine-Guaifenesin Oral Solution 10-100 mg/5 mL Antitussive Expectorant ,16 fl. oz…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What was recalled

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

Recalling firm
Woodfield Pharmaceutical, LLC
NDC code
58657-500-16
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0210-2018

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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