Class II · Moderate risk
Fosinopril Sodium and Hydrochlorothiazide Tablets
Subpotent; Hydrochlorothiazide at the 9 month time point.
Is Fosinopril recalled?
Not under an active recall.
Fosinopril was recalled 4 times in the past — all now closed. Most recent: Oct 11, 2013.
Most common reason: Labeling / mix-up (3 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Fosinopril. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Fosinopril recalls on record
none so far in 2026; 4 on record, newest first
Class II · Moderate risk
Fosinopril Sodium
Labeling: Label Mixup: FOSINOPRIL SODIUM, Tablet, 10 mg may have potentially been mislabeled as the following drug: MERCapsuleTOPURINE, Tablet, 50 mg, NDC 00054458111, Pedigree: AD54549_1, EXP: 5/20/2014.
Class II · Moderate risk
FOSINOPRIL SODIUM Tablet
Labeling:Label Mixup; FOSINOPRIL SODIUM, Tablet, 20 mg may be potentially mislabeled as TOLTERODINE TARTRATE ER, Capsule, 2 mg, NDC 00009519001, Pedigree: AD65478_1, EXP: 5/29/2014.
Class II · Moderate risk
FOSINOPRIL SODIUM Tablet
Labeling:Label Mixup; FOSINOPRIL SODIUM Tablet, 10 mg may be potentially mislabeled as CALCITRIOL, Capsule, 0.25 mcg, NDC 00054000725, Pedigree: AD46414_10, EXP: 5/16/2014.
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