Testosterone Cypionate Injection, USP, CIII, 200 mg/mL recall — FDA D-0489-2023
cGMP: complaints of crystals not redissolving into solution after warming and shaking the vials.
Overview of recall records associated with Azurity Pharmaceuticals, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
cGMP: complaints of crystals not redissolving into solution after warming and shaking the vials.
This page summarizes recall records in which the official source identifies Azurity Pharmaceuticals, Inc. 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.