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All product recalls associated with Guidant Corp-Cpi Division.
Total Recalls
13
Past Year
0
Class I (Serious)
0
Most Recent
Mar 2004
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 terminal hub component in a some of the catheters has an unintended abrupt transition between the entry port and the catheter lumen which can result in difficulty introducing or removing delivery system components during lead placement.
The terminal hub component in a some of the catheters has an unintended abrupt transition between the entry port and the catheter lumen which can result in difficulty introducing or removing delivery system components during lead placement.
Some of the pacemakers could have failed to pace due to an inadequately soldered electrical connection at an integrated circuit.