Devices

Device Recall StarBurst MRI SemiFlex Electrode Device

Model / Serial
Lot No. 4773676, 4776428 and 4780110
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - US Distribution to the states of AZ, AR, FL, MI, MN, MO, NY, TX, VA, WA and WI., and to the countries of Hungary and Spain.
Product Description
Starburst MRI Semi-Flex Electrode Device, 25cm/Attached Cable/14Ga/6.4F, Product No. H7877001039091, Catalog No. 700-103909; 25cm/14Ga/6.4F, Product No. H7877001026151, Catalog No. 700-102615; and 25cm/14Ga/6.4F, Product No. H7877001026151, Catalog No. 700-102615
Manufacturer
Angiodynamics
1 Event
- Recall of Device Recall StarBurst MRI SemiFlex Electrode Device

Manufacturer

Angiodynamics

Manufacturer Address
Angiodynamics, 10 Technical Park, Glens Falls NY 12804
Manufacturer Parent Company (2017)
AngioDynamics 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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