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All product recalls associated with GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland.
Total Recalls
382
Past Year
22
Class I (Serious)
2
Most Recent
Nov 2025
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.
There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.
There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.
GE HealthCare has become aware of an issue where information from two different patients can be mismatched when correcting patient or study information.