Diltiazem HCl Extended-release Capsules
Failed Impurities/Degradation Specifications; out of specification results for related compound per the manufacturer
Class III means the product is unlikely to cause harm but violates FDA labeling or manufacturing rules. These are the recalls you rarely hear about; pharmacies usually just swap the affected lot.
1,716 recalls, newest first.
Failed Impurities/Degradation Specifications; out of specification results for related compound per the manufacturer
Incorrect/Undeclared Excipient: There is a potential an incorrect grade of excipient was used during manufacturing.
Incorrect/Undeclared Excipient: There is a potential an incorrect grade of excipient was used during manufacturing.
Incorrect/Undeclared Excipient: There is a potential an incorrect grade of excipient was used during manufacturing.
Incorrect/Undeclared Excipient: There is a potential an incorrect grade of excipient was used during manufacturing.
Defective Container: Customer complaints of punctures in the bottle.
Failed Impurities/Degradation Specifications:out-of-specification (OOS) results for Azelastine N-oxide
Failed Impurities/Degradation Specifications: Out of specification test results obtained during routine stability testing for related compound.
Failed Impurities/Degradation Specifications: Out of specification test results obtained during routine stability testing for related compound.
Subpotent drug: The product active ingredient level not matching the exact levels indicated on the packaging label.
Subpotent Drug: low out of specification assay results for the octocrylene and avobenzone ingredients.
Subpotent Drug: low out of specification assay results for the octocrylene and avobenzone ingredients.
Failed Impurities/Degradation Specifications - OOS was observed for ATV Cyclo FP Impurity and Total Degradation Impurities tested at the 18 month stability time point in Atorvastatin Calcium Tablets 40 mg 500 tablets.
Superpotent Drug: High out of specification results for levofloxacin resulting in increased concentration of solution.
Superpotent Drug: High out of specification results for levofloxacin resulting in increased concentration of solution.
Superpotent Drug: High out of specification results for levofloxacin resulting in increased concentration of solution.
Failed Impurities/Degradation Specifications: An out-of-specification result in the related substance test during three month long-term stability study.
Labeling: Incorrect or Missing Lot and/or Exp Date: Incorrect expiration date on label
Superpotent Drug: lots out of specification for elevated sodium chloride and fluconazole assay.
Failed Stability Specifications: lot out of specification for elevated water vapor.
Superpotent Drug and Failed Stability Specifications: lot out of specification for elevated sodium chloride and elevated water vapor.
Labeling: Incorrect or Missing Lot and/or Exp Date: Product distributed without a lot number or expiration date on the outer carton.
Subpotent Drug
Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.
Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.