FOSINOPRIL SODIUM Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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.

What was recalled

FOSINOPRIL SODIUM Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505251002

Recalling firm: Aidapak Services, LLC
Origin: WA, United States
Initiated by: Voluntary: Firm initiated
FDA recall number: D-657-2014

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Fosinopril recalls

See all

Class II · Moderate risk Terminated Oct 11, 2013

Fosinopril Sodium and Hydrochlorothiazide Tablets, 10 mg/12.5 mg, Rx Only, 100 Tablets, Sandoz Inc. Princeton, NJ 08540 ---NDC…

Reason Subpotent; Hydrochlorothiazide at the 9 month time point.

Sandoz Inc NDC 0185-0341-01 D-393-2014

Class II · Moderate risk Terminated Jul 2, 2013