Lorazepam Tablets
Failed impurities/degradation specifications and Sub-potent Drug: Out-of-specification results were obtained during routine stability testing for Assay and Impurities.
Every FDA drug recall whose status is still Ongoing: the firm is still removing product from the market, or the FDA has not yet closed the file. Some were opened years ago and never formally terminated, so check the initiation date as well as the status.
2,760 recalls, newest first.
Failed impurities/degradation specifications and Sub-potent Drug: Out-of-specification results were obtained during routine stability testing for Assay and Impurities.
Out of Specification for Dissolution
cGMP Deviations: Product intended for quarantine was inadvertently distributed.
Failed Stability Specifications - 12-month stability test result for one of the known peptides is below the specification limit
Failed stability specifications: during routine stability monitoring quality concerns were identified. Physical separation for ingredients was observed.
Presence of Foreign Tablets/Capsules
CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended interim limit.
CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended interim limit.
CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended interim limit.
Presence of Particulate Matter: A market complaint was received of a glass piece in the vial.
Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain empty capsules
Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain empty capsules
CGMP Deviations; product intended for quarantine was inadvertently distributed
Labeling: Not Elsewhere Classified: misleading label similar in appearance to the FDA-approved drug product Adrenalin¿ (epinephrine injection, USP)
Failed Tablet/Capsule Specifications: Illegible product identification for the unit dose configuration only.
Non-Sterility
CGMP Deviations
LABELING: LABEL MIX-UP
LABELING: LABEL MIX-UP
Marketed without an Approved NDA/ANDA; FDA laboratory analysis confirmed product tainted with undeclared metformin and glyburide
Defective container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle
Presence of Foreign Tablets/Capsules
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.