Vencedor medicated balm
CGMP DEVIATIONS
775 recalls, newest first
CGMP DEVIATIONS
CGMP DEVIATIONS
Subpotent Drug
Failed Impurities Specification: Out-of-specification (OOS) stability test result was obtained for unspecified impurity.
Packaging defect: observed packaging defect, blister packaging inadequately sealed.
CGMP Deviations: Potential product carryover.
CGMP Deviations: Detection of N-Nitrosodimethylamine (NDMA) levels in excess of the Acceptable Daily Intake Limit.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
CGMP DEVIATIONS
CGMP DEVIATIONS
CGMP DEVIATIONS
CGMP DEVIATIONS
Labeling: Incorrect or Missing Lot and/or Exp Date
Presence of Foreign Tablets/Capsules: Pharmacist reported presence of some Gabapentin tablets 800 mg comingled in Gabapentin 600 mg 500 count bottles.
cGMP: complaints of crystals not redissolving into solution after warming and shaking the vials.
Failed Impurities/Degradation Specifications: Out of specification for related substance 10-hydroxy buprenorphine N-Oxide results generated at the 18-month stability timepoint.
Failed Impurities/Degradation Specifications: Out of specification for related substance 10-hydroxy buprenorphine N-Oxide results generated at the 18-month stability timepoint.
Failed Impurities/Degradation Specifications