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 Azurion 7 M12 System is a medical imaging device used in healthcare settings for various procedures. It is designed to assist healthcare providers in performing imaging diagnostics effectively.
The device may move unexpectedly when the Reset Geometry button is pressed, even with the table lock engaged. This defect can lead to unanticipated movements during critical medical procedures, posing a risk to patient safety.
This recall is not part of a broader industry pattern.
This recall affects healthcare providers and patients who rely on the Azurion 7 M12 System for medical imaging. The unexpected movement can lead to procedural complications and potential injuries.
Locate the model number and software version on the device's label or user manual.
Expect a response from Philips Medical Systems regarding refunds or replacements within 4-6 weeks.
Keep records of your device’s details, including model number and software version, as well as any correspondence with the manufacturer.
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.
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