Product Mix Up: This product is being recalled because of a complaint received that a sealed bottle of lisinopril and hydrochlorothiazide tablets 20mg/12.5 mg had a foreign tablet identified as atazanavir and ritonavir tablet 300mg/100mg.
Reason for recall: Product Mix Up: This product is being recalled because of a complaint received that a sealed bottle of lisinopril and hydrochlorothiazide tablets 20mg/12.5 mg had a foreign tablet identified as atazanavir and ritonavir tablet 300mg/100mg. Distribution: Product was distributed nationwide within the United States. Quantity: 58,968 bottles Lot/code info: Lot #: QA01081, Exp. Date April 2027
Official record: FDA (Drug enforcement) ↗
Republished from the official source above; details can change — the source record controls.