Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All Versions: R1.x, R2.x, R3.x
Azurion 7 B12 Recall Summary Philips is recalling certain Azurion 7 B12 medical imaging systems (model numbers 722067, 722225, and 722235 running software versions R1.X, R2.X, or R3.X) because the patient 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 specific system models and software versions.
- Recalling firm
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands
- Product
- Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; 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/c56dabb3-8c4c-4bd6-9a54-3ef0297d9ed1