ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025;
Pending LLM rewrite. Source: FDA_DEVICE Z-1666-2026.
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 Biplane OR Table; System Code: (1) 722020, (2)722025;
- 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 (8)
- (1) System Code: 722020
- UDI: N/A
- System Serial Number: 4
- (2) System Code: 722025
- UDI: 00884838059108
- System Serial Number: 6
- 2
- 3
Distribution
Distributed nationwide across the United States.
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