Simvastatin Tablets
Presence of foreign substance: metallic razor blade was found in one bottle.
165 recalls · Class III, newest first
Presence of foreign substance: metallic razor blade was found in one bottle.
Failed Content Uniformity Specifications
Subpotent Drug
Subpotent Drug
CGMP Deviations: Inadvertent release of a drug product with unapproved active ingredient manufacturer.
Presence of Foreign Substance: Reports have been received of damaged StripPax packets containing silica gel desiccant potentially allowing the silica gel granules to make contact with Auryxia tablets in the bottle.
Labeling: Label Error on Declared Strength. A single syringe labeled as 150 mg/1.0 mL was found packaged in a blister labeled as 120 mg/mL
Marketed without an Approved NDA/ANDA; product found to be tainted with sildenafil
Failed Impurities/Degradation Specifications: high out of specification test results obtained for individual and total impurities.
Failed Dissolution Specification
Failed Impurities/Degradation Specifications
Superpotent
Failed Stability Specifications
Superpotent
Failed Impurities/Degradation Specifications: high out of specification results for Dexamethasone adduct (related compound).
Failed Impurities/Degradation Specifications: high out of specification results for Dexamethasone adduct (related compound).
Failed Impurities/Degradation Specifications: Mylan Pharmaceuticals Inc. is conducting a voluntary recall due to related out of specification compound results obtained during routine stability testing.
Marketed without an approved NDA/ANDA: Bottles were released prior to final approval.
Labeling: Incorrect or Missing Lot and/or Exp Date; lot number on the secondary packaging doesnt match the lot number printed on the bottle
Failed Impurities/Degradation Specifications.
Failed Impurities/Degradation Specifications.
Failed Dissolution Specifications: Low out of specification results for dissolution.
Labeling: Incorrect or Missing Package Insert: authorized generic product was packaged with the incorrect insert for the brand name product Clolar (clofarabine) injection.
Labeling: Incorrect or Missing Package Insert.
Failed impurities/degradation specifications: Famotodine has an out of specification result for an individual related substance observed during routine stability testing of a batch for related substances -impurity 8 at 24 month stability interval.