Rizatriptan Benzoate Tablets USP
CGMP Deviations: N-Nitroso Desmethyl Rizatriptan Impurity results that are above the FDA acceptable limit.
Every FDA drug recall initiated in 2024, newest first, with its risk class, status and the reason the FDA recorded. Use the cause and risk filters to narrow the year down.
557 recalls, newest first.
CGMP Deviations: N-Nitroso Desmethyl Rizatriptan Impurity results that are above the FDA acceptable limit.
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Defective container: lack of seal integrity.
Failed Stability Specifications - at 12 months 2-8 degrees C followed by 6 weeks at 25 degrees C.
Presence of foreign substance: plastic-like substance.
Presence of Foreign Substance: metal in tablet
Presence of Foreign Tablets: Manufacturer received a report from a Pharmacist who reported finding a tablet of baclofen in a bottle of 1000-count tramadol
Failed Impurities/Degradation Specifications
Microbial Contamination of Non-Sterile Products - Presence of Acetobacter nitrogenifigens bacteria
Microbial Contamination of Non-Sterile Products - Presence of Acetobacter nitrogenifigens bacteria
Failed Impurities/Degradation Specifications
Failed Impurities/Degradation Specifications
Labeling: Wrong Barcode
Labeling: Label mix-up - ephedrine syringes mislabeled as phenylephrine.
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Presence of Foreign Tablets: Pharmacist reported a tablet of baclofen in a bottle of 1000-count tramadol
Presence of Particulate Matter: Potential for black particulates in the drug product.
Defective Container: yellow-colored spike from cap lodged in the nozzle. Firm received several complaints from customers.
Failed Tablet/Capsule Specifications: There is a potential for the imprint, M 122, to be missing on some tablets.
Presence of Foreign Substance; Broken metal piece found embedded in tablet.
Presence of Foreign Substance: This oil based product may contain trace amounts of water for injection (WFI).
Presence of foreign substance: Product complaint of foreign material in reconstituted bottle.
Presence of foreign substance: Product complaint of foreign material in reconstituted bottle.