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All product recalls associated with Actavis Inc.
Total Recalls
51
Past Year
0
Class I (Serious)
0
Most Recent
Feb 2017
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Failed Dissolution Specifications: Dissolution test results at 8 hour time-point were above approved specification limits.
Failed Impurities/Degradation Specifications
Failed Impurity/Degradation Specification; "Related Compound C"
Failed USP Dissolution Test Requirements: Out-of-specification dissolution results at the 8 hour stability testing point.
Failed Tablet/Capsule Specifications: Broken tablets
Failed Tablet/Capsule Specifications: Broken tablets
Failed Dissolution Specification: This product recall is due to the product lot # 50077231 exceeding dissolution specifications. All other test specifications were met.
Failed Dissolution Specifications; 8-hours for the 18-month stability testing point.
Impurities/Degradation Products: Recalled lots do not meet room temperature stability specification for unknown degradant.
Impurities/Degradation Products: Recalled lots do not meet room temperature stability specification for unknown degradant.
Subpotent; some patches may not contain fentanyl gel