Devices

Device Recall Recovery G2

Model / Serial
Lot numbers: GFPK3279, GFPK3280, GFPK3281 & GFPK3282
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
Yes
Distribution
Worldwide including USA, Australia, and Canada
Product Description
Recovery G2 Filter System - Jugular/Subclavian Delivery Kit, for use in the prevention of recurrent pulmonary embolism. Catalog Number RF-220J ***For Canada & Australia only***
Manufacturer
Bard Peripheral Vascular Inc
1 Event
- Recall of Device Recall Recovery G2

Manufacturer

Bard Peripheral Vascular Inc

Manufacturer Address
Bard Peripheral Vascular Inc, 1625 W 3rd St, Tempe AZ 85281-2438
Manufacturer Parent Company (2017)
Becton, Dickinson and Company
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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