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Devices
Device Recall Arrow Internationa IABP
Model / Serial
Lot Numbers: KF2073734 KS2083999 KF2083869 KF2083921
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution -- USA, Belgium, Great Britain, Italy, Kazakhstan, Latvia, Russia, Slovenia, Turkey, and South Africa.
Product Description
Arrow International FiberOptix Intra-Aortic Balloon Catheter Kit (IAB) 8 Fr 30 cc; || Product Number: IAB-05830-LWS. || The IAB is utilized for intra-aortic balloon counter-pulsation therapy.
Manufacturer
Arrow International Inc
1 Event
Recall of Device Recall Arrow Internationa IABP
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Manufacturer
Arrow International Inc
Manufacturer Address
Arrow International Inc, 2400 Bernville Road, Reading PA 19605
Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
USFDA
One device with a similar name
Learn more about the data
here
Device Recall Arrow Internationa IABP
Model / Serial
Lot Numbers: KF2073694 KF2083874 KF2083966 KF2094179 KF2073788 KF2083927 KF2084059
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution -- USA, Belgium, Great Britain, Italy, Kazakhstan, Latvia, Russia, Slovenia, Turkey, and South Africa.
Product Description
Arrow International FiberOptix Intra-Aortic Balloon Catheter Kit (IAB) 8 Fr 40 cc; || Product Number: IAB-05840-LWS. || The IAB is utilized for intra-aortic balloon counter-pulsation therapy.
Manufacturer
Arrow International Inc
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