Allura Xper FD20/20; System Code: 722038;
Pending LLM rewrite. Source: FDA_DEVICE Z-1669-2026.
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 FD20/20; System Code: 722038;
- 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: 722038
- UDI: 00884838054226
- System Serial Number: 71
- 115
- 42
- 108
- 173
- 119
- 60
- 37
- 38
- 99
- 130
- 48
- 157
- 41
- 141
- 137
- 49
- 63
Distribution
Distributed nationwide across the United States.
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