Reported Apr 8, 2026 · Ongoing
ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013;
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 Biplane
- System Code
(1) 722008(2)722013
- Lot codes and dates
- (1)
- System Code722008
- UDIN/A
- System Serial Number
144 of 144 codes
3603614452964873903061784202672452470491113386694133654543044421254413203251122544565234239407187437821022883491061054817142412361972641819192124483244224470279141459357287116
- System Code722013
- UDI00884838059061
- System Serial Number
318 of 318 codes
293424100174868346170218441249639290153410128951851962612614149637911542601214637360389303268264631254255515129156032783474265051094621491242162468447969105638375531404575
- Amount recalled
- 461 units (198 US, 263 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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