US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 1, 2012 (14 years ago)

CARDIOGEN-82 (Rubidium Rb 82 Generator), 140 millicurie, Rx Only, For Elution of sterile…

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

Why it was recalled

GMP deviation; Sr-82 levels exceeded alert limit specification

What was recalled

CARDIOGEN-82 (Rubidium Rb 82 Generator), 140 millicurie, Rx Only, For Elution of sterile nonpyrogenic Rubidium Chloride Rb 82, Manufactured for: Bracco Diagnostics Inc. Princeton, NJ 08543 by Medi-Physics, Inc. South Plainfield, NJ 07080, NDC 0270-0091-01

Recalling firm
Bracco Diagnostics Inc
NDC code
0270-0091-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1684-2012

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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