NORepinephrine Bitartrate
Subpotent Drug; confirmed results by FDA analysis after customer complaints of discoloration
142 recalls · Class III, newest first
Subpotent Drug; confirmed results by FDA analysis after customer complaints of discoloration
Subpotent Drug; confirmed results by FDA analysis after customer complaints of discoloration
Failed Impurities/Degradation Specifications; 9 month stability timepoint
Labeling: Label mix-up. Docusate Sodium 100mg Softgels were mislabeled as Docusate Calcium 240mg.
Failed Impurities/Degradation Specifications: Product recalled due to elevated impurity result detected during routine stability testing.
Defective Delivery System: Product may contain leaking capsules.
Super-Potent Drug: Out of Specification Assay test results were reported for stability samples.
Labeling: Incorrect or Missing Lot and/or Exp Date
Failed Impurities/Degradation Specifications; Impurity A
Failed Dissolution Specification
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Labeling: Not Elsewhere Classified: Lack of leaflets and approved labels on bottles.
Labeling: Not elsewhere classified. NDC number is incorrect on the container.
Failed Tablet/Capsule Specifications: Product recalled due to reports of breakage and leakage of Paricalcitol capsules.
Failed Tablet/Capsule Specifications: Product recalled due to reports of breakage and leakage of Paricalcitol capsules.
Failed Tablet/Capsule Specifications: Product recalled due to reports of breakage and leakage of Paricalcitol capsules.
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Failed Impurities/Degradation Specifications: Out of specifications results for impurities.
Failed Impurities/Degradation Specifications: Level of iron exceeds the limit set by the USP monograph for it (USP limit is NMT 0.5 ug/g (ppm)).
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Presence of Foreign Tablets/Capsules: one foreign capsule identified as omeprazole 10 mg was found in the bottle
Failed Stability Specifications: Out of Specification results obtained for preservative butylparaben.
Labeling: Incorrect or Missing Lot AND/OR Exp Date.