NDC 0363-6171-09 Walgreens Sinus Pressure
Boxes mislabeled to read "Decongestant Free", but the product contains Phenylephrine HCI 5mg
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.
Boxes mislabeled to read "Decongestant Free", but the product contains Phenylephrine HCI 5mg
Presence of Particulate Matter: Piece of metal found in a vial
Incorrect Product Formulation: Oxytocin 30 units was added to an IV bag of 0.45% Sodium Chloride (500mL) instead of 0.9% Sodium Chloride (500mL).
Product mix-up:0.2 mg strength Clonidine Hydrochloride Tablets, USP in a 100-count bottle of 0.3 mg strength Clonidine Hydrochloride Tablets,
Failed Viscosity specification: Slightly higher OOS results obtained for viscosity
Failed Stability Specifications: Out of specification results reported at 12-month stability testing for aluminum content.
Labeling: Not Elsewhere Classified - Incorrect label-incorrect scent listed on label.
Superpotent Drug: Assay value found to be 110.6% in Chlomipramine Hydrocholoride capsules
Failed Impurities/Degradation Specifications: Identification of an unknown impurity at the 12-month stability point.
Labeling: Not Elsewhere Classified: Carton incorrectly identifies product as doxylamine succinate HCl, however the product is doxylamine succinate.
Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
Defective Delivery System: An incorrect 10 mL (12 mL) Luer (slip) syringe packaged in one lot of Zynrelef 400 mg/12 mg kit
Subpotent Drug
Subpotent Drug - Out of specification (OOS) result obtained during monitoring stability study for Assay. Results below specification.
Labeling: Label Error on Declared Strength
Defective Container: Tube split from side seam
Labeling: Missing label: the product tube was missing a label and contained a different formulation.
Failed Dissolution Specifications
Failed Dissolution Specifications
Failed Tablet/Capsule Specification : Capsule breakage
Superpotent Drug: Out of specification for assay at the 12-month timepoint.
Superpotent Drug: Out of specification for assay at the 12-month timepoint.
Defective Container
Failed Impurities/Degradation Specifications; out-of-specification results for impurities obtained during routine stability testing