Doctor Manzanilla Allergy & Decongestant Relief Syrup recalled over manufacturing violations
- Recall date
- August 30, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Mid Valley Pharmaceutical recalls Doctor Manzanilla Allergy & Decongestant Relief (diphenhydramine hydrochloride and phenylephrine hydrochloride) Syrup,…
- Recall number
- D-1135-2017
- FDA classification
- Class II
- Brand / firm
- Mid Valley Pharmaceutical
- Sold / distributed
- TX
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.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
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.
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