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All product recalls associated with Edwards Lifesciences Research Medical, Inc..
Total Recalls
10
Past Year
0
Class I (Serious)
0
Most Recent
Sep 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.
Spontaneous balloon rupture during use of the product.
Balloon catheters were spontaneously rupturing during use.
Balloon rupture: Catheter balloon may rupture during cardiopulmonary bypass procedure. For further information, please telephone Edwards Lifesciences Research Medical, Inc. at 801-565-6173.