Prescription and over-the-counter medications
Cross contamination with other products: This sub-recall is being initiated in support of the recall by the manufacturer (Sandoz) dated 11/1/18, which included lots that were repackaged by American Health Packaging. Sandoz stated that "These lots are being recalled due to the potential presence of unrelated ingredients (i.e. traces of active ingredients of Benazepril, Haloperidol and Perphenazine), which were identified through a manufacturing investigation."
Right Value Drug Stores
Labeling Not Elsewhere Classified: Misbranding.
Cross Contamination with Other Products
Cross Contamination with Other Products
Right Value Drug Stores
Labeling Not Elsewhere Classified: Misbranding.
Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.
Failed pH Specifications: High Out-of-Specification results for pH were obtained during stability testing.
Zero Xtreme USA
Marketed Without an Approved NDA/ANDA: Undeclared Sibutramine
Taro Pharmaceuticals U.S.A.
Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.
Cross Contamination with Other Products
Taro Pharmaceuticals U.S.A.
Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.
Marketed Without An Approved NDA/ANDA: product contains undeclared sildenafil, tadalafil, and oxytetracycline, FDA approved drug products making Euphoric an unapproved drug.
Labeling: Missing label; potential for missing primary container label on the vial.
Right Value Drug Stores
Labeling Not Elsewhere Classified: Misbranding.
Takeda Development Center Americas
Failed Impurities/Degradation Specifications:Elevated levels of a known impurity in the 20-month stability sample testing.
Cross Contamination with Other Products
Right Value Drug Stores
Labeling Not Elsewhere Classified: Misbranding.
Cross Contamination with Other Products
Teva Pharmaceuticals USA
Failed Impurities/Degradation Specifications; out-of-specification results for impurities obtained during routine stability testing
Kadesh International
Non-Sterility: Product manufactured under non-sterile production conditions.