About the database
How to use the database
Download the data
FAQ
Credits
Manufacturers
Abbott Vascular-Cardiac Therapies dba Guidant Corporation
Manufacturer Address
Abbott Vascular-Cardiac Therapies dba Guidant Corporation, 26531 Ynez Rd, Temecula CA 92591-4630
Source
USFDA
17 Events
Recall of Device Recall ACS
Recall of Device Recall DUOSTAT
Recall of Device Recall ACS
Recall of Device Recall Guidant MultiLink RX Vision
Recall of Device Recall Abbott Vascular 6F Viking Guiding Catheter, Shape ALR 1.2
Recall of Device Recall Abbott Vascular 6F Viking Guiding Catheter, Shape BPL
Recall of Device Recall VOYAGER NC Coronary Dilatation Catheter
Recall of Device Recall VOYAGER NC Coronary Dilatation Catheter
Recall of Device Recall StarClose
Recall of Device Recall POWERSAIL
Recall of Device Recall POWERSAIL
Recall of Device Recall POWERSAIL
Recall of Device Recall POWERSAIL
Recall of Device Recall XACT Carotid Stent System
Recall of Device Recall Viatrac 14 Plus Peripheral Dilatation Catheter
Recall of Device Recall XACT Carotid Stent System
Recall of Device Recall RX ACCULINK Carotid Stent System
{{ $t('card.reduce') }}
{{ $tc('card.more', left) }}
17 devices in the database
Device Recall ACS
Model / Serial
6090751, 6090752, 6091151, 6091152
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide, including USA, Canada, Germany, Italy, Greece, New Zealand, Netherlands, France, Japan, Spain, and Bulgaria.
Product Description
ACS Rotating Hemostatic Valve, 0.096 inch, for use with a dilatation catheter - Reference Number 23242
Device Recall DUOSTAT
Model / Serial
6090551
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide, including USA, Canada, Germany, Italy, Greece, New Zealand, Netherlands, France, Japan, Spain, and Bulgaria.
Product Description
ACS DUOSTAT¿ Rotating Hemostatic Valve, 0.096 inch, for use with a dilatation catheter - Reference Number 23244
Device Recall ACS
Model / Serial
6090651, 6090652 , 6090653
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide, including USA, Canada, Germany, Italy, Greece, New Zealand, Netherlands, France, Japan, Spain, and Bulgaria.
Product Description
ACS Rotating Hemostatic Valve, .115 inch, for use with a dilatation catheter - Reference Number 23245
Device Recall Guidant MultiLink RX Vision
Model / Serial
Part number 1007848-15, lot number 7052951
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
Yes
Distribution
Nationwide
Product Description
Multi-Link Vision RX Coronary Stent System, 3.0 x 15mm, Part number 1007848-15, lot number 7052951
Device Recall Abbott Vascular 6F Viking Guiding Catheter, Shape ALR 1.2
Model / Serial
Lot Number: 8011791
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution.
Product Description
6F Viking Guiding Catheter, Percutaneous catheter, Shape ALR 1.2, Part Number: 1001934-06, Abbott Vascular, Santa Clara, CA 95054. || Designed to provide a pathway trough which therapeutic and diagnostic devices are introduced.
12 more
Language
English
Français
Español
한국어