ATHLETICARE Anti-Bacterial Hand Soap AC 550
Does Not Meet Monograph: product contains, triclosan, an ingredient that can no longer be contained in over-the-counter consumer antiseptic/antibacterial wash products.
1,525 recalls · Class III, newest first
Does Not Meet Monograph: product contains, triclosan, an ingredient that can no longer be contained in over-the-counter consumer antiseptic/antibacterial wash products.
Failed Dissolution Specifications
Failed Dissolution Specifications; 9-monthstability timepoint
Failed Impurities/Degradation Specifications: Expansion of July 2018 and February 2019 recall due to high out-of-specification for impurities.
Failed Dissolution Specifications
CGMP Deviations: Finished product made with lovastatin drug substance that was out of specification for individual impurity results.
Failed dissolution specifications
CGMP Deviations: Finished product made with lovastatin drug substance that was out of specification for individual impurity results.
Failed Degradation/Impurities Specifications: Out of specification related substance results during stability testing.
Failed Impurities/Degradation Specifications: High out of specification results obtained during routine stability testing
Labeling: Not Elsewhere Classified. Mometasone Furoate Cream has an NDC typographical error.
Discoloration: Esomeprazole Magnesium DR Capsules (40mg) may contain brown pellets.
Superpotent Drug: product may contain concentrations of oxytocin higher than what is represented on the label.
Superpotent Drug: product may contain concentrations of oxytocin higher than what is represented on the label.
Superpotent Drug: product may contain concentrations of oxytocin higher than what is represented on the label.
Failed Impurities/Degradation Specifications: Out of specification test results in related substance at three-month long term stability study was obtained.
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Failed Impurities/Degradation Specifications: OOS results observed in any other individual impurity and total impurities.
Failed Stability Specification; out of specification (OOS) results for a preservative at 9 month stability study.
Defective Container; complaints of leakage.
Labeling Not Elsewhere Classified: The front panel indicates 24 caplets whereas the side panel indicates 12 caplets. The drug product carton contains 24 caplets.