Devices

Device Recall GENICON EZEE

Model / Serial
Catalog No. 550-000-000; Lot No. I8095/2017-11-08, I8162-2018-01-09, I8162/2020-01-09; UDI: 00877972005223.
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Distributed domestically to FL, IL, MI, TN, UT. Distributed internationally to Dominican Republic, Ireland, Denmark, Spain, Switzerland, United Kingdom.
Product Description
GENICON EZEE Retrieval, sterile, Rx only.
Manufacturer
Genicon, Inc.
1 Event
- Recall of Device Recall GENICON EZEE

Manufacturer

Genicon, Inc.

Manufacturer Address
Genicon, Inc., 6869 Stapoint Ct Ste 112, Winter Park FL 32792-6603
Manufacturer Parent Company (2017)
Genicon Inc
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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