Devices

Device Recall AngioSeal

Model / Serial
Lot 1204437
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
No
Distribution
Nationwide.
Product Description
The affected device is labeled Angio-Seal Vascular Closure Device 6F VIP Platform, model 610130. The recalled product is the 6 French model size.
Manufacturer
St. Jude Medical / Daig Division
1 Event
- Recall of Device Recall AngioSeal

Manufacturer

St. Jude Medical / Daig Division

Manufacturer Address
St. Jude Medical / Daig Division, 14901 Deveau Pl, Minnetonka MN 55345-2126
Source
USFDA

One device with a similar name

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Device Recall AngioSeal Vascular Closure Device

Model / Serial
Lot number 1146548
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
No
Distribution
International Only-Belgium, China, Guadalajara, New Zealand and Thailand.
Product Description
Angio-Seal Vascular Closure Device. Ref 610109. 6F STS Platform. Sterilized by gamma radiation. For single use only. St. Jude Medical, Daig Division, Inc., Minnetonka, MN 55345-2126, USA.
Manufacturer
St. Jude Medical / Daig Division

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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