Recall database

Interventional Fluoroscopic X-Ray System recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 181–183 of 183 recalls

Class IIOngoingZ-1077-2025

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026

Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems.…

PHILIPS MEDICAL SYSTEM…Feb 12, 2025

Class IIOngoingZ-1076-2025

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura CV20 System Code: 722031

Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems.…

PHILIPS MEDICAL SYSTEM…Feb 12, 2025

Class IIOngoingZ-0922-2025

SIEMENS MEDICAL SOLUTIONS USA, INC recalls ARTIS One Angiographic X-Ray System

A potential issue with ARTIS One systems was identified. In very rare situations, the first x-ray release following patient registration may be performed with incorrect copper prefiltration.…

SIEMENS MEDICAL SOLUTI…Feb 5, 2025