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GE Healthcare GmbH Oskar-Schlemmer-Str. 11 Munich Germany

GE Healthcare GmbH Oskar-Schlemmer-Str. 11 Munich Germany Recalls

All product recalls associated with GE Healthcare GmbH Oskar-Schlemmer-Str. 11 Munich Germany.

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Recall Summary

Total Recalls

152

Past Year

22

Class I (Serious)

0

Most Recent

Nov 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–20 of 152 recalls

ViewPoint 6 (GE Healthcare) – incomplete patient history (2025)

GE HealthCare has become aware that the Patient History tab in ViewPoint 6 versions 6.15.3 and 6.15.4 ultrasound software may not include complete patient medical history information.

FDANov 3, 2025Nationwide• GE Healthcare GmbH Oskar-Schlemmer-Str. 11 Munich Germany

CARESCAPE ONE Monitor (GE) – battery performance (2025)

Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.

FDASep 26, 2025Nationwide• GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland

Carescape B450 Monitor (GE) – battery performance (2025)

Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.

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Moderate

FDASep 26, 2025Nationwide• GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland

Portrait VSM Monitor (GE) – battery performance (2025)

Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.

FDASep 26, 2025Nationwide• GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland

FLEX-3S2P Battery (GE) – battery performance (2025)

Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.

FDASep 26, 2025Nationwide• GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland

Patient Monitors B105/B125/B155 (GE) – battery performance (2025)

Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.

FDASep 26, 2025Nationwide• GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland

Carescape Central Station (Wipro GE Healthcare) – System Failure (2025)

GE HealthCare has identified an issue affecting Carescape" Central Station (CSCS) with software version V3.0.5, which can cause the system to enter a continuous reboot cycle. If this occurs, a loss of central monitoring of connected patients could result. This issue occurs only when the number of central stations connected to the network is 118, 119 or 120.

FDASep 5, 2025Nationwide• Wipro GE Healthcare Private Ltd. 122 Part 1 Odyssey And Galileo Bengaluru India

Change Healthcare Radiology Software (Change Healthcare) – Report Display Issue (2025)

Due to software issue, radiology reports may not be fully displayed when viewing.

FDAAug 13, 2025Nationwide• CHANGE HEALTHCARE CANADA COMPANY

Merge Hemo Software (Merge Healthcare) – patient data issue (2025)

Merge Healthcare has been informed by Schiller AG (Baar, Switzerland) of an issue with the Schiller ARGUS PB-3000 Patient Data Module (PDM) where certain units trigger an error message on the Merge Hemo Client (Pressure Sensor Defective) during non-invasive blood pressure (NIBP) measurements, specifically when the initial inflation pressure is set in the high-pressure range (>240 mmHg). The ARGUS PB-3000 is a vital signs monitoring instrument intended to be integrated into the Merge Hemo System. No other components of the Merge Hemo System are affected.

FDAAug 11, 2025Nationwide• Merge Healthcare, Inc.

Change Healthcare Cardiology Software (Change Healthcare) – Unexpected Shutdown (2025)

Due to complaints, software update may cause software to unexpectedly shutdown.

FDAMay 22, 2025Nationwide• CHANGE HEALTHCARE CANADA COMPANY

VERICIS Merge Cardio (Merge Healthcare) – Measurement Workflow Risk (2025)

When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may be inconsistent with the associated primitive measurements in the final patient report.

FDAFeb 19, 2025Nationwide• Merge Healthcare, Inc.

Centricity Cardiology CA1000 (GE Healthcare) – Security Vulnerability (2025)

There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.

FDAFeb 19, 2025Nationwide• GE Healthcare

Centricity Universal Viewer (GE Healthcare) – Security Vulnerability (2025)

There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.

FDAFeb 19, 2025Nationwide• GE Healthcare

Centricity PACS-IW (GE Healthcare) – Security Vulnerability (2025)

There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.

FDAFeb 19, 2025Nationwide• GE Healthcare

Merge Cardio (Merge Healthcare) – Measurement Workflow Issue (2025)

When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may be inconsistent with the associated primitive measurements in the final patient report.

FDAFeb 19, 2025Nationwide• Merge Healthcare, Inc.

Centricity Radiology RA600 (GE Healthcare) – Security Vulnerability (2025)

There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.

FDAFeb 19, 2025Nationwide• GE Healthcare

Centricity PACS-IW (GE Healthcare) – Security Vulnerability (2025)

There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.

FDAFeb 19, 2025Nationwide• GE Healthcare

SIGNA MR380 MRI System (GE Healthcare) – SAR monitoring (2025)

For certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" is above the limit indicated on the "SAR Display". The user interface may incorrectly enable a scan to proceed earlier than intended. If resumed by the operator, such a scan can result in potential excessive tissue heating, especially if the patient is in contact with a conductive material or has an implant.

FDAJan 31, 2025Nationwide• GE Healthcare (China) Co., Ltd. 1F-5F BLD 1, No.1 Tongji South Road, Beijing Economic-Technological Development Area Beijing China

SIGNA MR355/MR360 MRI System (GE Healthcare) – SAR monitoring (2025)

For certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" is above the limit indicated on the "SAR Display". The user interface may incorrectly enable a scan to proceed earlier than intended. If resumed by the operator, such a scan can result in potential excessive tissue heating, especially if the patient is in contact with a conductive material or has an implant.

FDAJan 31, 2025Nationwide• GE Healthcare (China) Co., Ltd. 1F-5F BLD 1, No.1 Tongji South Road, Beijing Economic-Technological Development Area Beijing China

Optima MR360 MRI System (GE Healthcare) – SAR monitoring (2025)

For certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" is above the limit indicated on the "SAR Display". The user interface may incorrectly enable a scan to proceed earlier than intended. If resumed by the operator, such a scan can result in potential excessive tissue heating, especially if the patient is in contact with a conductive material or has an implant.

FDAJan 31, 2025Nationwide• GE Healthcare (China) Co., Ltd. 1F-5F BLD 1, No.1 Tongji South Road, Beijing Economic-Technological Development Area Beijing China