Devices

Device Recall UNIFUSE INFUSION SYSTEM

Model / Serial
Lot 521372 (Use By 2013-07)
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution -- USA and The Netherlands.
Product Description
ANGIODYNAMICS UNI*FUSE INFUSION SYSTEM WITH COOPER WIRE, Catalog No./REF 12401819, CATHETER SIZE 4F, CATHETER LENGTH 90 cm, INFUSION LENGTH 20 cm, OCCLUSION WIRE SIZE .035 in., STERILE, AngioDynamics Inc., 603 Queensbury Avenue, Queensbury, NY 12804
Manufacturer
Angiodynamics Worldwide Headquarters
1 Event
- Recall of Device Recall UNIFUSE INFUSION SYSTEM

Manufacturer

Angiodynamics Worldwide Headquarters

Manufacturer Address
Angiodynamics Worldwide Headquarters, 14 Plaza Drive, Latham NY 12110-3421
Manufacturer Parent Company (2017)
AngioDynamics Inc
Source
USFDA

One device with a similar name

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Device Recall UNIFUSE INFUSION SYSTEM

Model / Serial
Lot 521388 (Use By 2013-07)
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution -- USA and The Netherlands.
Product Description
ANGIODYNAMICS UNI*FUSE INFUSION SYSTEM WITH COOPER WIRE, Catalog No./REF 12401818, CATHETER SIZE 4F, CATHETER LENGTH 90 cm, INFUSION LENGTH 10 cm, OCCLUSION WIRE SIZE .035 in., STERILE, AngioDynamics Inc., 603 Queensbury Avenue, Queensbury, NY 12804
Manufacturer
Angiodynamics Worldwide Headquarters

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Disclaimer

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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