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

Norpace CR (disopyramide phosphate) extended-release capsules USP,150 mg, packaged in a)…

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.

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