Reported Apr 8, 2026 · Ongoing
Allura Xper FD20/20; System Code: 722038;
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 FD20/20
- System Code722038
- Lot codes and dates
- System Code722038
- UDI00884838054226
- System Serial Number
111 of 111 codes
7111542108173119603738991304815741141137496335167557039624611867781207106102169118911740105113110513488641121439410973166147313127921353269121123
- Amount recalled
- 111 units (31 US, 80 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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