Philips Medical Systems recalled 1,979 Azurion 7 M12 Systems on January 26, 2026. The table may move unexpectedly when the Reset Geometry button is pressed, posing a high risk of injury. Healthcare providers and patients should stop using the devices immediately.
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. or your healthcare provider for instructions. Notification method: N/A
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The recall affects Azurion 7 M12 System models 722078, 722223, and 722233. All software versions R1.X, R2.X, and R3.X are included. The systems were distributed worldwide, with 365 units in the U.S. and 1,614 units internationally.
Under certain conditions, the Azurion 7 M12 System's table may move unexpectedly, even when the table lock is activated. This malfunction can lead to serious injury during medical procedures.
No specific injuries or incidents have been reported at this time. However, the potential for harm exists due to the unexpected movement of the device.
Stop using the Azurion 7 M12 System immediately. Contact Philips Medical Systems Nederland B.V. or your healthcare provider for further instructions.
For more information, contact Philips Medical Systems Nederland B.V. at their official website or through the recall notice linked below.
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