Oxycodone Hydrochloride Tablets
Out-of-specification impurity test result observed at 18-month long term stability time point.
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.
Out-of-specification impurity test result observed at 18-month long term stability time point.
Failed Stability Specifications: Out-of-specification results observed in a water loss test that might affect the assay content and alter drug concentration.
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Subpotent Drug: Product contains less Sodium Fluoride than listed on product label.
Labeling: Missing Label
Labeling: Missing Label
Superpotent; Hydrochlorothiazide
Subpotent Drug
Failed Impurities/Degradation Specifications
Failed dissolution specifications
Failed dissolution specifications
Failed dissolution specifications
Failed dissolution specifications
Failed dissolution specifications
Failed dissolution specifications
Failed dissolution specifications
Failed dissolution specifications
Failed dissolution specifications
Failed Impurities/Degradation Specifications
Discoloration