Cardiogen-82 recalls
Cardiogen-82 products have been recalled 1 time, most recently on 3 Oct 2012. The recalling company is usually Bracco Diagnostics. The most common reason is sterility.
Total recalls1since 2012
Last 12 months0reported
Class I00% of total
Ongoing0latest 3 Oct 2012
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 1 100%Class III 0 0%
Why cardiogen-82 is recalled
Companies
By year
All cardiogen-82 recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Cardiogen-82 (Rubidium Rb 82 Generator), 140 millicurie recalledCardiogen-82 | Bracco Diagnostics | Sterility | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.