DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose
Temperature Abuse: Product exposed to temperature outside specified limits.
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.
Temperature Abuse: Product exposed to temperature outside specified limits.
Failed Impurities/Degradation Specifications
Labeling: Incorrect or Missing Lot and/or Exp Date
Defective Container: complaints received regarding some incorrect press-in-bottle-adapters (PIBA), the incorrect PIBAs have a female instead of male fit so they cannot be used in combination with co-packed syringes.
Incorrect Product Formulation; product was manufactured with the incorrect Art Cherry Flavor flavoring agent instead of Art Black Cherry Flavor flavoring agent
Incorrect Product Formulation; product was manufactured with the incorrect Art Cherry Flavor flavoring agent instead of Art Black Cherry Flavor flavoring agent
Subpotent Drug
Failed Stability Specifications: product did not meet viscosity results.
Failed Moisture Limits: Out of specification for water content
Failed Impurities/Degradation Specifications
Labeling: Illegible label: Manufacturer received complaint of mis-alignment print of the printed dosing instructions on the blister card.
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
Temperature Abuse
Failed Impurity/Degradation Specifications: Out-of-specifications results observed for impurities during stability testing.
Failed pH specifications: Out of Specification pH results for 0.9% Sodium Chloride, USP
Subpotent
Labeling: Illegible label: Customer complaint received of mis-alignment print of the printed dosing instructions on the blister card.
Failed Impurities/Degradation Specifications:presence of ATV cyclo IP and FP, Dihydroxy epoxy and Dieto epoxy impurities
Temperature Abuse; labeled with the incorrect room temperature (15-25 ¿C) storage conditions rather than the correct refrigerated (2 - 8 ¿C) storage conditions
Failed Impurity/Degradation Specifications
Failed Impurities/ Degradation Specifications - OOS for know impurity Betamethasone 17- propionate.
Failed Impurities/ Degradation Specifications - OOS for know impurity Betamethasone 17- propionate.
Failed Impurities/ Degradation Specifications - OOS for know impurity Betamethasone 17- propionate.