Reported Jun 24, 2026 · Ongoing
Philips Allura Xper with the following Model Numbers: Model # 722001 for Allura Xper FD10C; Model # 722002 for Allura…
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 4-6 · Best · N/A
Is this the product you have?
26 of 26 products
| Model / number | Product as published |
|---|---|
722001 | Philips Allura Xper with the following Model Numbers: for Allura Xper FD10C |
722002 | for Allura Xper FD10F |
722003 | for Allura Xper FD10 |
722005 | for Allura Xper FD10/10 |
722006 | for Allura Xper FD20 |
722008 | for Allura Xper FD20 Biplane |
722010 | for Allura Xper FD10 |
722011 | for Allura Xper FD10/10 |
722012 | for Allura Xper FD20 |
722013 | for Allura Xper FD20 Biplane |
722015 | for Allura Xper FD20 OR Table |
722019 | for Allura Xper FD10/10 OR Table |
722020 | for Allura Xper FD20 Biplane OR Table |
722022 | for Allura Xper FD10 OR Table |
722023 | for Allura Xper FD20 OR Table |
722025 | for Allura Xper FD20 Biplane OR Table |
722026 | for Allura Xper FD10 |
722027 | for Allura Xper FD10/10 |
722028 | for Allura Xper FD20 |
722029 | for Allura Xper FD20/10 |
- Lot codes and dates
- All codes
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Why it was recalled
Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and additional contrast injection
This product could cause temporary or reversible health problems — stop using it.
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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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