PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Azurion R2.1 - Class 2 Recall
Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of the affected system. Affected PCs: XRay PC, Suite PC, and FlexViewing PC Azurion Model Name - Model Number: Azurion 3 M12 722063 722221; Azurion 3 M15 722064 722222; Azurion 5 M20 722228; Azurion 7 B12 722067 722225; Azurion 7 B20 722068 722226; Azurion 7 M12 722078 722223; Azurion 7 M20 722079 722224; (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 17, 2024 Category: Medical Devices Source Type: alerts

XRAY PAIN RELIEF (menthol, (plus)-, camphor, (-)-, and methyl salicylate) cream [Genomma Lab USA]
Updated Date: Fri, 29 Dec 2023 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - December 29, 2023 Category: Drugs & Pharmacology Source Type: alerts

Carestream Health, Inc. - DRX Revolution Mobile XRay System - Class 2 Recall
DRX Revolution Mobile X-Ray System (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 2, 2023 Category: Medical Devices Source Type: alerts

Philips Medical Systems Nederland B.V. - Interventional fluoroscopic xray system - Class 2 Recall
Allura Xper series (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 8, 2023 Category: Medical Devices Source Type: alerts

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Allura Xper and Azurion Interventional Fluoroscopic XRay Systems - Class 2 Recall
Wireless Foot Switch distributed with Philips Allura Xper and Azurion Interventional Fluoroscopic X-Ray Systems (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 31, 2023 Category: Medical Devices Source Type: alerts

GE OEC Medical Systems, Inc - Imageintensified fluoroscopic xray system, mobile - Class 2 Recall
OEC 9900 Systems with 9-inch Image Intensifier (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 1, 2023 Category: Medical Devices Source Type: alerts

SEDECAL SA - Mobile Digital Diagnostic XRay System - Class 2 Recall
wDR 2.2 Mobile Digital Diagnostic X-Ray System (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 1, 2023 Category: Medical Devices Source Type: alerts

NeuroLogica Corporation - Samsung GM85 Digital Xray Imaging System - Class 2 Recall
Samsung GM85 Digital X-ray Imaging System-A Digital Diagnostic Mobile X-ray System (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 20, 2023 Category: Medical Devices Source Type: alerts

FUJIFILM Healthcare Americas Corporation - Supria Wholebody Xray CT System - Class 2 Recall
Surpria: Software Version V3.11, V3.22 (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 17, 2022 Category: Medical Devices Source Type: alerts

FUJIFILM Healthcare Americas Corporation - Supria 64 Wholebody Xray CT System - Class 2 Recall
Surpria 64: Software Version V3.11, V3.22 (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 17, 2022 Category: Medical Devices Source Type: alerts

XRAY DOL (camphor, menthol, and methyl salicylate) cream [Genomma Lab USA, Inc.]
Updated Date: Mon, 06 Jun 2022 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - June 6, 2022 Category: Drugs & Pharmacology Source Type: alerts

Shimadzu Medical Systems - XRAY TV SYSTEM SONIALVISION G4 - Class 2 Recall
MODEL: X-RAY TV SYSTEM SONIALVISION G4 (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 8, 2022 Category: Medical Devices Source Type: alerts

Philips North America Llc - Interventional Fluoroscopic Xray System - Class 2 Recall
Philips Allura (Model Numbers 722010, 722012, 722026, 722027, 722028, 722029, 722035) and Philips Azurion (Model Numbers 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222, 722223, 722224, 722225, 722226, 722227, 722228) running StentBoost Live (Model Number 459801781661) Software Version Number: R2.0 (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 7, 2022 Category: Medical Devices Source Type: alerts

Philips North America Llc - Philips Azurion Interventional Fluoroscopic XRay System - Class 2 Recall
Philips Azurion Interventional Fluoroscopic X-Ray System, Software version 2.1.x, Model numbers 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222, 722223, 722224, 722225, 722226, 722227, 722228. (Azurion 3 M12, Azurion 3 M15, Azurion 5 M12, Azurion 5 M20, Azurion 7 B12, Azurion 7 B20, Azurion 7 M12, Azurion 7 M20) (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 10, 2021 Category: Medical Devices Source Type: alerts

GE Healthcare, LLC - AMX Navigate Mobile XRay System - Class 2 Recall
AMX Navigate (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 30, 2021 Category: Medical Devices Source Type: alerts