St. Jude Medical Atrial Fibrillation Division Inc
Sunnyvale, CA
This page shows every FDA and USDA recall linked to St. Jude Medical Atrial Fibrillation Division Inc. Each entry includes the product involved, when the recall happened, and how serious it was. If a company has had multiple recalls over the years, you can see the full history here in one place — including whether any were Class I, which is the most serious type.
1
Total Recalls
2009
First Recall
2010
Most Recent
St. Jude Medical Epicor UltraWand LP Handheld Ablation Device, model UW-LP-2, Sterilized with Ethylene Oxide....
Jun 7, 2010
· Device
Terminated