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All product recalls associated with Apotex Inc..
Total Recalls
45
Past Year
0
Class I (Serious)
2
Most Recent
May 2020
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Chemical Contamination: Product were manufactured with active pharmaceutical ingredient (API) batches contaminated with residual materials and solvents.
Failed Impurities/Degradation Specifications: Out of Specification for an impurity at the 18 month stability time point.
Presence of Particulate Matter: Product from lot KF2199, may contain tablets with pieces of nitrile rubber glove embedded within the tablets.
Lack of Assurance of Sterility: Failed at expiry for Preservative Effectiveness Test (PET), therefore the product may be susceptible to microbial growth before the expiry date.
Presence of Particulate Matter: Lots identified in this recall notification may contain small particulates.