Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;
Pending LLM rewrite. Source: FDA_DEVICE Z-1675-2026.
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 7 B12; System Code: (1)722067, (2)722225, (3)722235;
- 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: 722067
- UDI: 00884838085350
- System Serial Number: 221
- 42
- 172
- 173
- 109
- 250
- 103
- 192
- 92
- 114
- 225
- 69
- 214
- 41
- 98
- 81
- 123
- 278
Distribution
Distributed nationwide across the United States.
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