Azurion 7 M20 System Model Numbers: (1)722079, (2)722224, (3)722234, (4)722282(OUS only); Software
Pending LLM rewrite. Source: FDA_DEVICE Z-1349-2026.
Severity not yet assessed
We have not scored this recall against our rubric yet, so we are not showing a severity rating or our usual guidance. The agency’s own notice below is the authoritative source — read it first.
Plain-English summary
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
The recalled product
- 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
- Manufacturer
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Category
- Medical Device — Devices
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (9)
- System Model Numbers: (1)722079
- (2)722224
- (3)722234
- (4)722282(OUS only)
- UDI-DIs: (1)884838085268
- (2)884838099258
- (3)884838116771
- (4)N/A
- Serial Numbers: All
Distribution
Distributed nationwide across the United States.
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