Devices

Device Recall AngioJet XVG Thrombectomy Catheter

Model / Serial
71851, 71852, 71997, 72086, 72539, 73170, 73171, 73646, 73758.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
AR, AZ, CA, FL, GA, IL, IN, KS, KY, MA, ME, MI, MN, MO, MS, NC, NH, NJ, NY, OH, OR, PA, SC, TN, TX, WA, WI, WV
Product Description
Possis AngioJet XVG Thrombectomy Sets, || Model/Order # 105042-001, Sterilized with Ethylene Oxide, || Possis Medical, Inc., 9055 Evergreen Boulevard NW, Minneapolis, MN 55433-8003. (These sets are used with the new AngioJet Ultra Console)
Manufacturer
Possis Medical, Inc
1 Event
- Recall of Device Recall AngioJet XVG Thrombectomy Catheter

Manufacturer

Possis Medical, Inc

Manufacturer Address
Possis Medical, Inc, 9055 Evergreen Blvd Nw, Minneapolis MN 55433-5833
Source
USFDA

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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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