Pharmakon Pharmaceuticals Morphine Sulfate 0.5 mg/mL, Preservative Free in 0.9% Sodium recall — FDA D-0871-2016
Super-Potent Drug: Out of specification for potency results (high) were obtained for one lot of morphine sulfate Inj.
Overview of recall records associated with Pharmakon Pharmaceuticals, including dates, categories and classifications where available.
Classification mix: Class I: 3.
Super-Potent Drug: Out of specification for potency results (high) were obtained for one lot of morphine sulfate Inj.
Incorrect/ Undeclared Excipient: Contains undeclared benzyl alcohol.
Incorrect/ Undeclared Excipient: Contains undeclared benzyl alcohol.
This page summarizes recall records in which the official source identifies Pharmakon Pharmaceuticals 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.