Devices

Device Recall Cordis Aquatrack

Model / Serial
Lots 80000521 and 80000584
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide distribution.
Product Description
Cordis Aquatrack Hydrophilic Nitinol Guidewire, for use in angiographic procedures, REF C3526-SSA, Guidewire Diameter .035" Tip Length Flexible 3 cm, Sterile. || Contents 5 Hydrophilic guidewires and torquing devices.
Manufacturer
Cordis Corporation
1 Event
- Recall of Device Recall Cordis Aquatrack

Manufacturer

Cordis Corporation

Manufacturer Address
Cordis Corporation, 14201 Nw 60th Ave, Miami Lakes FL 33014-2802
Manufacturer Parent Company (2017)
Cardinal Health
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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