GE Healthcare recalls Revolution CT and Revolution CT ES CT scanners due to potential inaccurate dose display in specific situations, which could lead to incorrect radiation exposure assessments.
The accumulated dose is incorrectly displayed in certain situations. There are two situations that will result in the SmartStep displayed dose being inaccurately high.
GE Healthcare is recalling Revolution CT and Revolution: CT ES scanners because they may display an incorrectly high radiation dose in certain situations. This could lead to patients receiving more radiation than intended, though the risk is not immediate or severe.
The scanner may show a higher radiation dose than actually delivered in specific situations. This could lead to patients being exposed to more radiation than necessary, potentially increasing health risks.
Patients using these CT scanners for medical imaging. Individuals who receive scans from these machines may be at risk of receiving more radiation than intended.
Check for Revolution CT or Revolution CT ES models. These scanners were sold by GE Healthcare for medical imaging.
Identify your scanner model to confirm if it is a recalled Revolution CT or Revolution CT ES.
The recall indicates a potential for inaccurate dose display, but it does not specify immediate danger or serious injury risk. The risk is considered low.
Check if your scanner is labeled as Revolution CT or Revolution CT ES. These models were sold by GE Healthcare for medical imaging.
The recall does not provide a specific remedy, so you should check with GE Healthcare to confirm if your scanner is affected.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0816-2022 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-0816-2022 from GE Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
