Azurion 7 M20 System Model Numbers: (1)722079, (2)722224, (3)722234, (4)722282(ous Only); Software Version Number - All Versions: R1.x, R2.x, R3.x
Philips is recalling certain Azurion 7 M20 imaging systems because the patient table may move unexpectedly when the Reset Geometry button is pressed, even if the table lock is engaged. This affects systems with model numbers 722079, 722224, 722234, and 722282, running any R1.X, R2.X, or R3.X software versions. The recall applies to Azurion 7 M20 systems used in healthcare facilities.
- Recalling firm
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands
- Product
- Azurion 7 M20 System Model Numbers: (1)722079, (2)722224, (3)722234, (4)722282(OUS only); 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/bc20d8f6-a2ed-4efe-9351-34afd61f0a95