Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;
Pending LLM rewrite. Source: FDA_DEVICE Z-1677-2026.
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 M12; System Code: (1)722078, (2)722223, (3)722233;
- 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: 722078
- UDI: 00884838085251
- System Serial Number: 302
- 585
- 410
- 753
- 523
- 293
- 840
- 291
- 536
- 537
- 870
- 613
- 598
- 679
- 224
- 829
- 249
- 546
Distribution
Distributed nationwide across the United States.
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