Azurion 7 B20 System Model Numbers: (1)722068, (2)722226, (3)722236; Software Version Number - All Versions: R1.x, R2.x, R3.x
Recall Summary Philips is recalling Azurion 7 B20 imaging systems (model numbers 722068, 722226, and 722236) running any R1.X, R2.X, or R3.X software version because the examination table may move unexpectedly when the Reset Geometry button is pressed, even when the table lock is engaged. This recall affects medical facilities using these systems.
- Recalling firm
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands
- Product
- Azurion 7 B20 System Model Numbers: (1)722068, (2)722226, (3)722236; 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/466d605f-afa0-4b55-ace4-e96c58fa9b78