Sense XL Torso Coil

2024: Recognition of marriage in scanners

At the end of June 2024, Philips announced the presence of a defect in its magnetic resonance imaging (MRI) devices. The defect can lead to fires, as well as provoke second or third degree burns in patients.

The problem is related to the first generation Sense XL Torso Coil. It is a 16-element article that is used in body and abdominal imaging in the Philips MR Intera and Achieva systems. The U.S. Food and Drug Administration (FDA) has given the defect a maximum hazard rating: meaning the devices can cause patients "serious injury or death.

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WSJ

The coils can be subjected to excessive local heating during scanning: in this case, there is a possibility of injury to the patient. Philips ceased production of the first generation Sense XL Torso Coil in 2014. However, the issue reportedly affects about 1,050 devices worldwide. As of April 2024, 64 complaints were registered, including 52 reports of harm to patients.

The affected devices can continue to be used in accordance with operating instructions and additional recommendations, the manufacturer's notice says.

Medical institutions, in particular, should be used when scanning special pads/mattresses. The study time should not exceed 45 minutes. Philips is developing a solution that fixes the problem. A software update may be released to limit scan settings. The introduction of structural changes is also not excluded. At the same time, the company emphasizes that maintaining a high level of safety and quality of products is its top priority.^[1]

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