Azurion 5 M12 System Model Numbers: (1)722227, (2)722231; Software Version Number - All Versions: R1.x, R2.x, R3.x
Recall Summary Philips is recalling Azurion 5 M12 medical imaging systems (model numbers 722227 and 722231) with software versions R1.X, R2.X, or R3.X because the examination table may move unexpectedly when the Reset Geometry button is pressed, even if the table lock is engaged. This recall affects healthcare facilities using these systems.
- Recalling firm
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands
- Product
- Azurion 5 M12 System Model Numbers: (1)722227, (2)722231; 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/6fed09bd-44c4-4098-bffc-89b84ddf92f5