Reported Apr 8, 2026 · Ongoing
Allura Xper FD20/15; System Code: 722058;
Philips Medical Systems Nederland B.v.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · Veenpluis 6 · Best · N/A
Is this the product you have?
- Allura Xper FD20/15
- System Code722058
- Lot codes and dates
- System Code722058
- UDI00884838059115
- System Serial Number
296 of 296 codes
100239305259203373111382329012427434036616218641961562852776516856178138212249257337265109134712381902191973252412331937861205149264167365199278215288254943042791718285
- Amount recalled
- 296 units (68 US, 228 OUS)
This recall covers 23 products
The agency filed one notice per product. You are reading one of them; the other 22 are below.
10 more are in the archive.
Where it was sold
- Nationwide
- GA
Why it was recalled
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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