St. Jude Medical Daig Division The affected device is labeled Angio-Seal Vascular Closure Device 6F VIP Platform, model 610130. The recalled product is the 6 French model size. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
The affected device is labeled Angio-Seal Vascular Closure Device 6F VIP Platform, model 610130. The recalled product is the 6 French model size.
Brand
St. Jude Medical Daig Division
Lot Codes / Batch Numbers
Lot 1204437
Products Sold
Lot 1204437
St. Jude Medical Daig Division is recalling The affected device is labeled Angio-Seal Vascular Closure Device 6F VIP Platform, model 610130. Th due to The Angio Seal VIP 6F devices were incorrectly packaged with a 0.038'' guidewire vs. the required 0.035'' guidewire.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The Angio Seal VIP 6F devices were incorrectly packaged with a 0.038'' guidewire vs. the required 0.035'' guidewire.
Recommended Action
Per FDA guidance
All consignees were notified by letter on June 7, 2006. All product is to be retreived by recalling firm''s sales force for return to St. Jude Medical, in Minnetonka, MN.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026