Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
INTELERAD MEDICAL SYSTEMS INCORPORATED 800, Boul. de Maisonneuve Est 12th floor Montreal Canada

INTELERAD MEDICAL SYSTEMS INCORPORATED 800, Boul. de Maisonneuve Est 12th floor Montreal Canada Recalls

All product recalls associated with INTELERAD MEDICAL SYSTEMS INCORPORATED 800, Boul. de Maisonneuve Est 12th floor Montreal Canada.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

353

Class I (Serious)

Most Recent

Jan 2026

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 101–120 of 3680 recalls

IntelePACS (Intelerad) – Software Communication Bug (2025)

Software application that receives digital images and data to be communicated, processed, manipulated, enhanced, stored, displayed has a bug that could cause data loss in Relevant Clinical Info field when modifying studies through Case Editor in either Technologist Portal or Referring Physician Portal, which could result in loss of clinical information, which could impact clinical decision-making.

Moderate

FDAOct 17, 2025Nationwide• INTELERAD MEDICAL SYSTEMS INCORPORATED 800, Boul. de Maisonneuve Est 12th floor Montreal Canada

VANTAGE GALAN 3T (Canon Medical) – Electrode Distance Compliance (2025)

Affected system contains components that do not meet the required distance between electrodes for compliance with the IEC 60601-1 standard for medical electrical equipment.

Moderate

FDAOct 16, 2025NV, OH• Canon Medical System, USA, INC.

Ceiling Type X-Ray Tube Support (Shimadzu) – Mounting Shaft Risk (2025)

Due to an issue (potential breakage) with the shaft for the mounting of the X-ray tube assembly that could potentially result assembly coming off the rotating shaft.

1...4 567 8...184

Page 6 of 184Next

High

FDAOct 16, 2025Nationwide• SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Nishinokyo Kuwabara Cho Nakagyo-Ku

ACUSON Imaging Catheter (Sterilmed) – reprocessing cycles (2025)

Affected catheters were reprocessed beyond validated cycles. This may compromise device sterility or mechanical integrity of the device and can lead to severe adverse events such as infection, vascular injury or embolism.

Moderate

FDAOct 8, 2025Nationwide• Sterilmed, Inc.

ACUSON ACUNAV Catheter (Sterilmed) – Reprocessing Integrity Risk (2025)

Moderate

FDAOct 8, 2025Nationwide• Sterilmed, Inc.

MC3 VitalFlow Console (Medtronic) – error code issue (2025)

As of August 6, 2025, Medtronic has received eleven reports of VitalFlow Consoles displaying an E70 error code during normal operation. When this occurs, the touch screen may become temporarily unresponsive and go blank for up to two minutes before recovering to full functionality. Importantly, the console continues to maintain set pump speed and function throughout.

Low

FDAOct 3, 2025Nationwide• Medtronic Perfusion Systems

ProxiDiagnost N90 (Philips) – carriage movement issue (2025)

Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.

Moderate

FDAOct 1, 2025Nationwide• Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany

Zenition 50 X-ray System (Philips) – image quality degradation (2025)

Over time some systems may experience loss of imaging functionality and/or poor image quality due to potential corrosion of the Image Intensifier Television (IITV) control board.

Moderate

FDASep 29, 2025MO, TX• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Incisive CT (Philips) – movement control issue (2025)

Laceration Risk

Issue 1: The potential for unintentional continued gantry/couch movement when a specific button series is used requiring use of manual stop. Issue 2. When performing a helical/Axial scan with ORI (Dose Right index)/ DOM (Dose Modulation), the WED (Water Equivalent Diameter) value might set itself to zero, and this may lead to an insufficient dose setting after the surview. If operator misses the insufficient dose and the WED value in User Interface and continues with the subsequent helical/Axial scans, then the obtained images will be noisy due to low dose setting. Issue 3: Due to a software failure, the ECG wave file is not saved. As a result, the cardiac offline image reconstruction fails due to the missing ECG wave file, and the user might rescan the patient. Issue 4: This issue is software fault in which the patient orientation will be changed to NULL under specific random scenarios resulting in radiation being delivered from the wrong orientation (surview scan) or in the wrong position (clinical scan) and will generate incorrect and undiagnosable surview/clinical images. Patients may be rescanned for surview and/or clinical images. Issue 5: During scanning, the preview image display is not consistent, the images are not arriving at a fixed rate, skipping images from time to time during scanning. The obtained images might not support making the clinical diagnosis and the user might decide to re-scan the patient. Issue 6: If a user presses the left and middle/right mouse buttons together or afterwards in a short time, both commands are executed and an incorrect auto ROI is created. This ROI coordinates won t be assigned as the object is empty. As a result, the threshold of contrast level will not be reached in the UI and this will prevent the system from automatically triggering the subsequent clinical scan. There is potential safety risk identified for additionally tracker shots and/or rescan of a patient when the clinical scan is not triggered. This issue only affects the manual ROI process.

Moderate

FDASep 25, 2025AL, AR, CA +15 more• PHILIPS MEDICAL SYSTEMS

CT 5300 (Philips) – movement control issue (2025)

Laceration Risk

Moderate

FDASep 25, 2025AL, AR, CA +15 more• PHILIPS MEDICAL SYSTEMS

Incisive CT Brazil (Philips) – movement control issue (2025)

Laceration Risk

High

FDASep 25, 2025AL, AR, CA +15 more• PHILIPS MEDICAL SYSTEMS

LOGIQ P9 Ultrasound (GE Medical) – Measurement Inaccuracy (2025)

The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.

Moderate

FDASep 18, 2025Nationwide• GE Medical Systems, LLC

LOGIQ P10 Ultrasound (GE Medical) – Measurement Inaccuracy (2025)

Moderate

FDASep 18, 2025Nationwide• GE Medical Systems, LLC

LOGIQ P10 HD Ultrasound (GE Medical) – Measurement Inaccuracy (2025)

Moderate

FDASep 18, 2025Nationwide• GE Medical Systems, LLC

Kirkland Signature Ahi Tuna Wasabi Poke – Listeria Contamination (2025)

Listeria

Listeria monocytogenes. Recall was initiated after being notified by green onion supplier of a Listeria monocytogenes positive test result in the green onions which were used only in Ahi Tuna Wasabi Poke.

Class IHigh

FDASep 18, 2025AL, AK, AR +34 more• Western United Fish Company Inc

Millenium MPR (GE Medical) – Service End Risk (2025)

GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.

Very High

FDASep 12, 2025Nationwide• GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING 9, Andrey Sakharov Haifa Israel

Stay Informed

INTELERAD MEDICAL SYSTEMS INCORPORATED 800, Boul. de Maisonneuve Est 12th floor Montreal Canada Recalls

Recall Summary

IntelePACS (Intelerad) – Software Communication Bug (2025)

VANTAGE GALAN 3T (Canon Medical) – Electrode Distance Compliance (2025)

Ceiling Type X-Ray Tube Support (Shimadzu) – Mounting Shaft Risk (2025)

ACUSON Imaging Catheter (Sterilmed) – reprocessing cycles (2025)

ACUSON ACUNAV Catheter (Sterilmed) – Reprocessing Integrity Risk (2025)

MC3 VitalFlow Console (Medtronic) – error code issue (2025)

ProxiDiagnost N90 (Philips) – carriage movement issue (2025)

CombiDiagnost R90 (Philips) – carriage movement issue (2025)

DigitalDiagnost 4 (Philips) – carriage movement issue (2025)

Precision CRF System (Philips) – carriage movement issue (2025)

Radiography 7300 C (Philips) – carriage movement issue (2025)

Zenition 50 X-ray System (Philips) – image quality degradation (2025)

Incisive CT (Philips) – movement control issue (2025)

CT 5300 (Philips) – movement control issue (2025)

Incisive CT Brazil (Philips) – movement control issue (2025)

LOGIQ P9 Ultrasound (GE Medical) – Measurement Inaccuracy (2025)

LOGIQ P10 Ultrasound (GE Medical) – Measurement Inaccuracy (2025)

LOGIQ P10 HD Ultrasound (GE Medical) – Measurement Inaccuracy (2025)

Kirkland Signature Ahi Tuna Wasabi Poke – Listeria Contamination (2025)

Millenium MPR (GE Medical) – Service End Risk (2025)