Mid Valley Pharmaceutical Doctor Manzanilla Allergy & Decongestant Relief recall — FDA D-1135-2017
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
Overview of recall records associated with Mid Valley Pharmaceutical, including dates, categories and classifications where available.
Classification mix: Class II: 2.
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
This page summarizes recall records in which the official source identifies Mid Valley Pharmaceutical as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.