atropine Sulfate Injection
Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
1,464 recalls · Class II, newest first
Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Labeling: Label Error on Declared Strength: Label incorrectly identifies product dose as 5ml instead of 10 ml.
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
cGMP Deviations
cGMP Deviations; Clonidine hydrochloride drug substance used in the manufacturing of this product, was dispensed in unauthorized rooms by the drug substance manufacturer
cGMP Deviations; Clonidine hydrochloride drug substance used in the manufacturing of this product, was dispensed in unauthorized rooms by the drug substance manufacturer
cGMP Deviations; Clonidine hydrochloride drug substance used in the manufacturing of this product, was dispensed in unauthorized rooms by the drug substance manufacturer
Failed Impurities/Degradation Specifications: Two lots failed specification for unknown impurity at the 24 month stability testing.
Failed Impurities/Degradation Specifications: failed specification for unknown impurity at the 24 month stability testing.
Presence of Particulate Matter and Lack of Assurance of Sterility: The firm received a complaint for customer of presence of particulate matter, leaky containers, and missing port protectors.
Lack of assurance of sterility: Potential channel leaks near the threaded vial port.
Crystallization; identified as calcium salt of Ketorolac
Crystallization; identified as calcium salt of Ketorolac
Failed Dissolution Specifications: low out-of-specification (OOS) results for dissolution were obtained at the nine-month stability point.
Lack of Assurance of Sterility: Due to lack of documentation of proper environmental monitoring during the time in which the medication was produced.
Lack of Assurance of Sterility: Due to lack of documentation of proper environmental monitoring during the time in which the medication was produced.
Lack of Assurance of Sterility: Due to lack of documentation of proper environmental monitoring during the time in which the medication was produced.