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Loose Cable Leads To Class I Recall For GE Ventilator

A loose cable found in certain models of GE anesthesia machines has resulted in the highest recall alert from the US FDA. Regulators are warning the mechanical problem could result in organ failure and even death.

Care Station 2 recall by FDA
• Source: GE Healthcare/ Shutterstock

The US Food and Drug Administration has issued a high-risk class I recall for GE Healthcare's Carestation 600 anesthesia systems due to a mechanical problem found in the devices that could cause serious harm to patients – and potentially be fatal.

The machines are meant to help children and adult patients undergoing anesthesia with breathing support. They are used by hospitals,...

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