The Recall Desk

FDA (Devices) recall action 99223

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalled 2 products on 2026-06-24

The FDA (Devices) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.

Products
2
Announced
2026-06-24
Critical
0
Units
—

Why these products were 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

The agency’s own wording, quoted from the enforcement report.

1–2 of 2

  • HighFDA (Devices)··2026-06-24

    Philips Allura Xper hand switch buttons may not fully release

    Philips Allura Xper and MultiDiagnost Eleva systems are being recalled because the hand switch button may not fully release, potentially causing loss of imaging or unintended radiation exposure.

    Product
    Philips Allura Xper with the following Model Numbers: Model # 722001 for Allura Xper FD10C; Model # 722002 for Allura Xper FD10F; Model # 722003 for Allura Xper FD10; Model # 722005 for Allura Xper FD10/10; Model # 722006 for Allura Xper FD20; Model # 722008 for Allura Xper FD20
    Category
    Distribution
    0 states
  • HighFDA (Devices)··2026-06-24

    Philips MultiDiagnost Eleva hand switch buttons may not fully release

    Philips MultiDiagnost Eleva systems are being recalled because the hand switch button may not fully release, potentially causing loss of imaging or unintended radiation exposure.

    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 # 70803
    Category
    Distribution
    0 states