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All product recalls associated with GE Medical Systems, LLC.
Total Recalls
1000
Past Year
1000
Class I (Serious)
34
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.
GE Healthcare has recently become aware of an error in the generator software on the Revolution XR/d configured with HP 8200 PC consoles that reports a mAs reading that is higher than is actually exposed to patients.
Package sterile barrier may be breached, compromising sterility.
A software error causes the wedge accessory calculation to be ignored in the radiotherapy treatment plan.