US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 30, 2017 (9 years ago)

Doctor Manzanilla Allergy & Decongestant Relief (diphenhydramine hydrochloride and…

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

Why it was recalled

CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.

What was recalled

Doctor Manzanilla Allergy & Decongestant Relief (diphenhydramine hydrochloride and phenylephrine hydrochloride) Syrup, 12.5 mg and 5 mg in each 5 mL, 4 fl oz. (118 mL) bottle, Distributed by: Midvalley Pharmaceuticals, Raymondville, TX 78580, UPC 7 62558 00204 1.

Recalling firm
Mid Valley Pharmaceutical
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1135-2017

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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