US Drug Recall Register
Class III · Low risk Terminated Initiated Dec 2, 2015 (11 years ago)

Norpace CR

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Dissolution Specification

What was recalled

Norpace CR (disopyramide phosphate) extended-release capsules USP,150 mg, packaged in a) 100-count bottles (NDC 0025-2742-31), and b) 500-count bottles (NDC 0025-2742-51), Rx only, Distributed by G.D. Searle LLC, Division of Pfizer Inc, NY, NY 10017.

Recalling firm
Pfizer Inc.
NDC code
0025-2742-31
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0520-2016

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 Disopyramide recalls

See all
Class II · Moderate risk Terminated

Disopyramide Phosphate

Reason Labeling: Label Mixup: DISOPYRAMIDE PHOSPHATE, Capsule, 150 mg may have potentially been mislabeled as the following drug: THYROID, Tablet, 30 mg, NDC 00456045801, Pedigree: AD65323_1, EXP: 5/29/2014.

Aidapak Services, LLC D-836-2014
Class III · Low risk Terminated

Norpace CR

Reason Failed Dissolution Specification

Pfizer Inc NDC 0025-2742-31 D-607-2013