Allura Xper FD20/10; System Code: 722029;
Pending LLM rewrite. Source: FDA_DEVICE Z-1668-2026.
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 FD20/10; System Code: 722029;
- 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)
- System Code: 722029
- UDI: 00884838059078
- System Serial Number: 57
- 7
- 88
- 56
- 126
- 94
- 30
- 31
- 21
- 97
- 91
- 110
- 100
- 63
- 60
- 55
- 62
- 129
Distribution
Distributed nationwide across the United States.
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