La Vita Compounding Pharmacy Methyl Folate CA+ 1mg/ml Injection w/Pres recall — FDA D-0922-2018
Lack of Processing Controls: products produced in a manner that calls into question the sterility of the drug product intended to be sterile.
Overview of recall records associated with La Vita Compounding Pharmacy, LLC, including dates, categories and classifications where available.
Classification mix: Class II: 3.
Lack of Processing Controls: products produced in a manner that calls into question the sterility of the drug product intended to be sterile.
Lack of Processing Controls: products produced in a manner that calls into question the sterility of the drug product intended to be sterile.
Lack of Processing Controls: products produced in a manner that calls into question the sterility of the drug product intended to be sterile.
This page summarizes recall records in which the official source identifies La Vita Compounding Pharmacy, LLC 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.