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All product recalls associated with Heartport, Inc. Route.
Total Recalls
5
Past Year
0
Class I (Serious)
0
Most Recent
Apr 2005
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.
Guidewire is protruding through the film portion of the packages which compromises the sterility of the device.
Damaged hemostasis valves that prevent or present difficulty when inserting catheters.
Damaged hemostasis valves that prevent or present difficulty when inserting catheters.
Damaged hemostasis valves that prevent or present difficulty when inserting catheters.