Overview of recall records associated with Zydus Pharmaceuticals (USA) Inc, including dates, categories and classifications where available.
Classification mix: Class II: 29, Class III: 2.
Failed Impurities/Degradation Specifications: Out-of-Specification test results obtained for any individual unknown degradation product during Related Compounds testing during long term…
Failed Impurities/Degradation Specifications: Out-of-Specification test results obtained for any individual unknown degradation product during Related Compounds testing during long term…
CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity above the recommended interim limit
Presence of Foreign Substance: Product complaint received for the presence of foreign material embedded resembling a metal shaving in one tablet.
Failed Impurities/Degradation Specifications
Failed Impurities/Degradation Specifications
Labeling: Not Elsewhere Classified - Wrong NDC number
This page summarizes recall records in which the official source identifies Zydus Pharmaceuticals (USA) 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.
