ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)722023, (3)722035;
Pending LLM rewrite. Source: FDA_DEVICE Z-1665-2026.
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 OR Table; System Code: (1) 722015, (2)722023, (3)722035;
- 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: 722015
- UDI: N/A
- System Serial Number: 12
- 16
- 2
- 8
- 23
- 3
- 13
- (2) System Code: 722023
- UDI: 00884838059085
- System Serial Number: 49
- 41
- 142
- 110
- 12
- 179
- 124
- 27
- 98
Distribution
Distributed nationwide across the United States.
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