Fentanyl Citrate Inj., USP, CII, 250 mcg/5 mL (50 mcg/mL) (0.05 mg/mL) recall — FDA D-1139-2015
Failed Impurities/Degradation Specifications; 12 month stability testing (Expansion of RES #70548).
Overview of recall records associated with West-Ward Pharmaceutical Corp., including dates, categories and classifications where available.
Classification mix: Class III: 1.
Failed Impurities/Degradation Specifications; 12 month stability testing (Expansion of RES #70548).
This page summarizes recall records in which the official source identifies West-Ward Pharmaceutical Corp. 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.