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All product recalls associated with Abbott Vascular-Cardiac Therapies dba Guidant Corporation.
Total Recalls
57
Past Year
0
Class I (Serious)
0
Most Recent
Oct 2009
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The recall was initiated after Abbott Vascular discovered, through internal testing, that the affected lot may not meet our quality specifications for catheter shaft tensile strength.
Distal shaft of the POWERSAIL coronary Dilatation Catheters exhibits damage that may result in a leak of contrast material and functional failures.
Potential sterility issue. Internal component quarantined for possible contamination, was released for sale after going through sterilization procedure.