Philips Medical Systems recalled 1,503 Azurion 7 B20 systems on January 26, 2026. The devices may move unexpectedly when the Reset Geometry button is pressed, posing a risk of injury. Healthcare providers must stop using the device and follow recall instructions 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 B20 System is a medical imaging table used in various diagnostic and surgical settings. It is designed to support patients during procedures requiring imaging technology.
The defect allows the table to move unpredictably, even with a lock engaged, which can jeopardize patient safety during procedures.
This recall is not part of a broader industry pattern.
The recall poses a significant safety risk to patients and healthcare providers, necessitating immediate action to prevent injuries.
Model numbers are typically located on the device's identification label, usually found on the back or bottom of the table.
Expect a refund or replacement processing timeline of 4-6 weeks after the recall is acknowledged.
Keep a record of all communications regarding the recall, including emails, call logs, and any response from Philips Medical Systems.
The recalled models include Azurion 7 B20 System Model Numbers: 722068, 722226, and 722236. They were distributed worldwide, with 326 units in the U.S. and 1,177 units internationally. The devices have all software version numbers: R1.X, R2.X, R3.X.
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