US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 2, 2013 (13 years ago)

ISOSORBIDE DINITRATE ER Tablet

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

Why it was recalled

Labeling:Label Mixup; ISOSORBIDE DINITRATE ER Tablet, 40 mg may be potentially mislabeled as CILOSTAZOL, Tablet, 50 mg, NDC 60505252101, Pedigree: AD21811_7, EXP: 5/1/2014.

What was recalled

ISOSORBIDE DINITRATE ER Tablet, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 57664060088

Recalling firm
Aidapak Services, LLC
Origin
WA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-631-2014

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 Isosorbide recalls

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Class II · Moderate risk Terminated

Isosorbide Dinitrate Tablets

Reason Cross Contamination with Other Products

Sandoz Inc NDC 68001-222-00 D-0261-2019
Class II · Moderate risk Terminated

Isosorbide Dinitrate Tablets

Reason Cross Contamination with Other Products

Sandoz Inc NDC 68001-225-00 D-0260-2019
Class II · Moderate risk Terminated

Isosorbide Dinitrate Tablets

Reason Cross Contamination with Other Products

Sandoz Inc NDC 68001-223-00 D-0259-2019
Class II · Moderate risk Terminated

Isosorbide Dinitrate Tablets

Reason Cross Contamination with Other Products

Sandoz Inc NDC 0781-1695-01 D-0258-2019
Class II · Moderate risk Terminated

Isosorbide Dinitrate active pharmaceutical ingredient packaged in…

Reason Penicillin Cross Contamination: All lots of all products repackaged and distributed between 01/05/12 and 02/12/15 are being recalled because they were repackaged in a facility with penicillin products without adequate separation which could introduce the potential for cross contamination with penicillin.

Attix Pharmaceuticals D-737-2015