4 FDA recalls mention Fosinopril. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Fosinopril.
Reason Subpotent; Hydrochlorothiazide at the 9 month time point.
Reason Labeling: Label Mixup: FOSINOPRIL SODIUM, Tablet, 10 mg may have potentially been mislabeled as the following drug: MERCapsuleTOPURINE, Tablet, 50…
Reason Labeling:Label Mixup; FOSINOPRIL SODIUM, Tablet, 20 mg may be potentially mislabeled as TOLTERODINE TARTRATE ER, Capsule, 2 mg, NDC 00009519001…
Reason Labeling:Label Mixup; FOSINOPRIL SODIUM Tablet, 10 mg may be potentially mislabeled as CALCITRIOL, Capsule, 0.25 mcg, NDC 00054000725, Pedigree…
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