St. Jude Medical Daig Division
Minnetonka, MN
This page shows every FDA and USDA recall linked to St. Jude Medical Daig Division. 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.
5
Total Recalls
2005
First Recall
2007
Most Recent
FastCath Transseptal Catheter Introducers with Hemostasis Valve, DAIG division of St. Jude Medical, Minnetonka...
Mar 1, 2007
· Device
Terminated
The affected device is labeled Angio-Seal Vascular Closure Device 6F VIP Platform, model 610130. The recalled...
Nov 7, 2006
· Device
Terminated
St. Jude AGILIS Steerable Introducer, Reorder number 408304 and 408308 (Australia). Sterile EO. St. Jude Medi...
Jun 3, 2006
· Device
Terminated
Angio-Seal Vascular Closure Device. Ref 610109. 6F STS Platform. Sterilized by gamma radiation. For single...
Mar 25, 2006
· Device
Terminated
Sheath Obturator, introducer, catheter. Obturator Accessory Kit Reorder number 406405, a 6 Fr, 15 cm length O...
Nov 3, 2005
· Device
Terminated