All recalls8,521 total
Firm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.
Firm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.
Firm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.
Glazed ceramic plates are recalled because they may exceed FDA guidance levels for leachable lead (3.0mg/L).
Glazed ceramic plates are recalled because they may exceed FDA guidance levels for leachable lead (3.0mg/L).
Failed Impurities/Degradation Specifications: Product is being recalled due to API related substances and unknown impurities that are above the specification limits.
Failed Dissolution Specifications: results below specifications
Toxic levels of muscimol
Toxic levels of muscimol
Toxic levels of muscimol
Toxic levels of muscimol
Toxic levels of muscimol
Toxic levels of muscimol
Toxic levels of muscimol
Toxic levels of muscimol
Toxic levels of muscimol
Toxic levels of muscimol
Toxic levels of muscimol
Toxic levels of muscimol
Toxic levels of muscimol
Toxic levels of muscimol
Toxic levels of muscimol
Toxic levels of muscimol
Potential contamination with Salmonella
Toxic levels of muscimol
Toxic levels of muscimol
Toxic levels of muscimol
Toxic levels of muscimol
Potential contamination with Salmonella
Potential contamination with Salmonella
Toxic levels of muscimol
Toxic levels of muscimol
Presence of particulate matter: glass
Potential Salmonella contamination.
CGMP Deviations: Out of specification for dissolution
CGMP Deviations: Manufactured without following Current Good Manufacturing Practises.
Marketed without an approved NDA/ANDA: FDA analysis found product to be tainted with undeclared acetaminophen, diclofenac, and phenylbutazone.
Labeling: Incorrect or Missing Lot and/or Exp Date. Missing lot number and expiration dates on packets
Product sample exceeded tolerance for pesticide Fenvalerate
Failed Dissolution Specifications
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Undeclared milk
Undeclared Walnut
Product is recalled due to potential mold growth contamination.
Undeclared milk
Product is recalled due to potential mold growth contamination.
Failed Dissolution Specifications; the product is dissolving faster than the specified limits.