FDAFDA recall Z-2411-2026 · Jun 24, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips MultiDiagnost Eleva with the following Model Numbers: Model # 708032 for MultiDiag recall
Recall found
Product
Philips MultiDiagnost Eleva with the following Model Numbers: Model # 708032 for MultiDiagnost Eleva; Model # 708034 for MultiDiagnost Eleva with Flat Detector; Model # 708036 for MultiDiagnost Eleva; Model # 708037 for MultiDiagnost Eleva with Flat Detector; Model # 708038 for MultiDiagnost Eleva with Flat Detector.
Reason for recall
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
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- All codes
- Distribution
- US and ROW.
- Recalling firm
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., Best
- Voluntary or mandated
- FDA Mandated
- Recall started
- 2026-05-18
Source: openFDA enforcement record Z-2411-2026 · search recall number Z-2411-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.