Azurion 3 M12 System Model Numbers: (1) 722063, (2) 722221, (3) 722229; Software Version Number - All Versions: R1.x, R2.x, R3.x
Summary Philips is recalling Azurion 3 M12 imaging systems (model numbers 722063, 722221, and 722229) with software versions R1.X, R2.X, or R3.X because the patient table may move unexpectedly when the Reset Geometry button is pressed, even when the table lock is engaged. This recall affects medical facilities that use these systems.
- Recalling firm
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands
- Product
- Azurion 3 M12 System Model Numbers: (1) 722063, (2) 722221, (3) 722229; Software Version Number - All versions: R1.X, R2.X, R3.X
- Reason
- Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
- Classification
- Class II
- Category
- consumer product recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-01-26
- Status
- Open, Classified
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/a3055b57-d3c9-40b4-891b-2c6872be30c3