Allura Xper FD20/15; System Code: 722058;
Pending LLM rewrite. Source: FDA_DEVICE Z-1671-2026.
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 FD20/15; System Code: 722058;
- 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: 722058
- UDI: 00884838059115
- System Serial Number: 100
- 239
- 305
- 259
- 203
- 373
- 111
- 38
- 23
- 290
- 124
- 274
- 340
- 366
- 162
- 186
- 4
- 196
Distribution
Distributed nationwide across the United States.
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