Devices

Device Recall AngioJet XMI RX

Model / Serial
model number: 105421-002, Lot number 56594
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Lot was distributed to 3 OUS distributors located in Italy, United Kingdom and Netherlands.
Product Description
AngioJet XMI Rapid Exchange +, 4F, 135 cm. Contents: One (1) Thrombectomy Catheter for Peripheral Use. Sterilized with Ethylene Oxide. Single Use Only. Manufactured and Distributed by: Possis Medical, Inc. 9055 Evergreen Boulevard NW, Minneapolis, MN 55433-8003 USA.
Manufacturer
Possis Medical, Inc
1 Event
- Recall of Device Recall AngioJet XMI RX

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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