Cyclophosphamide Injection 500 mg/5 mL (100 mg/mL), Hazardous Drug recall — FDA D-0651-2025
cGMP deviations: Temperature excursion during transportation.
Overview of recall records associated with Sandoz Inc, including dates, categories and classifications where available.
Classification mix: Class I: 2, Class II: 1.
cGMP deviations: Temperature excursion during transportation.
Labeling: Label Mix-Up; cartons of Cefazolin for Injection, USP 1 gram were found to contain vials labeled as penicillin G potassium for Injection, USP, 20 million Unit. The vials contained…
Labeling: Label Mix-Up; Some vials of Cefazolin for Injection, USP 1 gram were incorrectly labeled as penicillin G potassium for Injection, USP, 20 million Unit
This page summarizes recall records in which the official source identifies Sandoz 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.