sulfur8 medicated LIGHT FORMULA
Subpotent Drug: failed at the 3 and 6 month stability time points.
1,525 recalls · Class III, newest first
Subpotent Drug: failed at the 3 and 6 month stability time points.
Labeling: Label Mix-Up
CGMP Deviations: Cylinders filled using out of date gauges.
Labeling: Incorrect or Missing Lot and/or Exp Date: some vials may be mislabeled with an incorrect "Compounded" date, lot number, and "Do Not Use Beyond" date or BUD (Before Use Date) that may be longer than intended.
Failed Impurities/Degradation Specifications: out of specification result for known impurity at 6 month timepoint.
Failed Impurities/Degradation Specifications
Failed Impurities/Degradation Specifications
Failed Impurities/Degradation Specifications
Failed Impurities/Degradation Specifications
Failed Dissolution Specification: Out of specification dissolution results when testing product stability.
Failed Dissolution Specification: Out of specification dissolution results when testing product stability.
Failed Dissolution Specification: Out of specification dissolution results when testing product stability.
Failed Impurities/Degradation Specifications; 9 month stability (manufacturer)
Labeling: Incorrect or Missing Package Insert: Package insert is missing updates compared with reference drug insert.
Labeling: Incorrect or Missing Package Insert: Package insert is missing updates compared with reference drug insert.
Labeling: Incorrect or Missing Package Insert: Package insert is missing updates compared with reference drug insert.
Tablets/Capsules Imprinted with Wrong ID; product debossed with an incorrect punch. Bottles could contain tablets debossed with V259 (debossing for PreTab) instead of the correct punch, V264 (debossing for Virt-Nate).
Failed Impurities/Degradation Specifications: Out of specification for a known degradant.
Subpotent Drug; confirmed results by FDA analysis after customer complaints of discoloration
Subpotent Drug; confirmed results by FDA analysis after customer complaints of discoloration
Failed Impurities/Degradation Specifications; 9 month stability timepoint
Labeling: Label mix-up. Docusate Sodium 100mg Softgels were mislabeled as Docusate Calcium 240mg.
Failed Impurities/Degradation Specifications: Product recalled due to elevated impurity result detected during routine stability testing.
Defective Delivery System: Product may contain leaking capsules.
Super-Potent Drug: Out of Specification Assay test results were reported for stability samples.