Reported Apr 8, 2026 · Ongoing
ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;
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 FD10/10
- System Code
(1) 722005(2)722011(3)722027
- Lot codes and dates
- (1)
- System Code722005
- UDIN/A
- System Serial Number
113 of 113 codes
321285490512983294936132335545631616930556541926925834647449753026152338438827123336727042734339936021225111252070392128357485405306307467234287333533209369543332328366389538394
- System Code722011
- UDI00884838059047
- System Serial Number
176 of 176 codes
491373753321021039510738013217115727036276792223430834324177848231917133168345344835915170163101255173325871554015421527322220321422024216671156361863002133724155
- System Code722027
- UDI00884838054196
- System Serial Number
273 of 273 codes
351332171319431012950112240241175298280107183202164153335288342134156265306307152106169203234209267284263127116174394956120123133305246255401781044226618732132828218453
- Amount recalled
- 112 units (138 US, 422 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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