Reported Jun 24, 2026 · Ongoing
Philips MultiDiagnost Eleva with the following Model Numbers: Model # 708032 for MultiDiagnost Eleva; Model # 708034…
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?
5 of 5 products
| Model / number | Product as published |
|---|---|
708032 | Philips MultiDiagnost Eleva with the following Model Numbers: for MultiDiagnost Eleva |
708034 | for MultiDiagnost Eleva with Flat Detector |
708036 | for MultiDiagnost Eleva |
708037 | for MultiDiagnost Eleva with Flat Detector |
708038 | for MultiDiagnost Eleva with Flat Detector. |
- 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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