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All product recalls associated with GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland.
Total Recalls
1000
Past Year
426
Class I (Serious)
54
Most Recent
Jan 2026
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.
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.
Store-made deli items contain a pasta ingredient that was recalled due to potential Listeria monocytogenes
Store-made deli items contain a pasta ingredient that was recalled due to potential Listeria monocytogenes