ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;
Pending LLM rewrite. Source: FDA_DEVICE Z-1662-2026.
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
- ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;
- 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: 722005
- UDI: N/A
- System Serial Number: 321
- 285
- 490
- 51
- 298
- 329
- 49
- 361
- 323
- 355
- 456
- 316
- 169
- 305
- 565
- 419
- 269
- 258
Distribution
Distributed nationwide across the United States.
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