ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;
Pending LLM rewrite. Source: FDA_DEVICE Z-1661-2026.
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 FD10; System Code: (1) 722003, (2)722010, (3)722026;
- 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: 722003
- UDI: N/A
- System Serial Number: 445
- 1555
- 1084
- 1411
- 1232
- 1259
- 1023
- 1947
- 392
- 1133
- 1135
- 1627
- 746
- 98
- 1078
- 367
- 1584
- 1599
Distribution
Distributed nationwide across the United States.
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