Azurion 3 M12; System Code: (1)722063, (2)722221, (3)722229;
Pending LLM rewrite. Source: FDA_DEVICE Z-1673-2026.
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
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
The recalled product
- Product
- Azurion 3 M12; System Code: (1)722063, (2)722221, (3)722229;
- 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 (20)
- (1) System Code: 722063
- UDI: 00884838085275
- System Serial Number:122
- 56
- 64
- 131
- 84
- 132
- 96
- 98
- 108
- 77
- 82
- 145
- 47
- 146
- 80
- 102
- 43
- 117
Distribution
Distributed nationwide across the United States.
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