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Canon Medical System, USA, INC.

Canon Medical System, USA, INC. Recalls

All product recalls associated with Canon Medical System, USA, INC..

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Recall Summary

Total Recalls

1000

Past Year

888

Class I (Serious)

124

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 5381–5400 of 17593 recalls

INFX-8000V System (Canon Medical) – X-Ray Field Shift (2021)

The x-ray irradiation field may shift with respect to image receiving surface displayed on the screen at some C-arm angles.

Moderate

FDAFeb 5, 2021Nationwide• Canon Medical System, USA, INC.

INFX-8000C System (Canon Medical) – X-Ray Field Shift (2021)

The x-ray irradiation field may shift with respect to image receiving surface displayed on the screen at some C-arm angles.

Moderate

FDAFeb 5, 2021Nationwide• Canon Medical System, USA, INC.

Panang Curry Sauce (Barbara's Orchard) – Undeclared Shrimp (2021)

Undeclared Allergen

Undeclared allergen: Shrimp

Class IHigh

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FDA

Feb 5, 2021

CO, FL, IL +5 more

• Barbara's Orchard/Delicae Gourmet

Thai Peanut Sauce (Barbara's Orchard) – Undeclared Shrimp (2021)

Undeclared Allergen

Undeclared allergen: Shrimp

Class IHigh

FDAFeb 5, 2021CO, FL, IL +5 more• Barbara's Orchard/Delicae Gourmet

Spicy Red Curry Sauce (Barbara's Orchard) – Undeclared Shrimp (2021)

Undeclared Allergen

Undeclared allergen: Shrimp

Class IHigh

FDAFeb 5, 2021CO, FL, IL +5 more• Barbara's Orchard/Delicae Gourmet

Custom Perfusion System (Medtronic) – Bacterial Endotoxin Risk (2021)

Laceration Risk

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

High

FDAFeb 4, 2021Nationwide• Medtronic Perfusion Systems

Medtronic Infant Tubing Set (Medtronic) – Bacterial Endotoxin Risk (2021)

Laceration Risk

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

High

FDAFeb 4, 2021Nationwide• Medtronic Perfusion Systems

Cummins X15 Engine (Cummins) – Flywheel Attachment Issue (2021)

Cummins, Inc. (Cummins) is recalling certain X15 diesel engines, part number D103109BX03. The capscrews that attach the flywheel to the crankshaft may have been improperly torqued, allowing the flywheel to detach.

High

NHTSAFeb 4, 2021Nationwide• CUMMINS

Medtronic Kinderset Pack (Medtronic) – Bacterial Endotoxin Risk (2021)

Laceration Risk

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

High

FDAFeb 4, 2021Nationwide• Medtronic Perfusion Systems

Medtronic Affinity Pixie Oxygenator (Medtronic) – Bacterial Endotoxin Risk (2021)

Laceration Risk

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

High

FDAFeb 4, 2021Nationwide• Medtronic Perfusion Systems

Medtronic Custom Pediatric Set (Medtronic) – Bacterial Endotoxin Risk (2021)

Laceration Risk

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

High

FDAFeb 4, 2021Nationwide• Medtronic Perfusion Systems

Medtronic EVNP Clinical Pack (Medtronic) – Bacterial Endotoxin Risk (2021)

Laceration Risk

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

High

FDAFeb 4, 2021Nationwide• Medtronic Perfusion Systems

Medtronic Custom Perfusion Pack (Medtronic) – Bacterial Endotoxin Risk (2021)

Laceration Risk

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

High

FDAFeb 4, 2021Nationwide• Medtronic Perfusion Systems

Medtronic Affinity Pixie Oxygenator (Medtronic) – Bacterial Endotoxin Risk (2021)

Laceration Risk

Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.

High

FDAFeb 4, 2021Nationwide• Medtronic Perfusion Systems

Thread-Like Wire Marker (Somatex) – Wire Splintering Risk (2021)

This recall has been initiated due to the risk of wire splintering after contact with a cautery device during the removal of a lesion. There is a potential risk that wire fragments are not removed during the procedure and stays inside the patient's body.

High

FDAFeb 3, 2021MO, NJ, OH• Somatex Medical Technologies GMBH Hohenzollerndamm 150-151 Berlin Germany

Medtronic ICD Devices (Medtronic) – Replacement Time Concern (2021)

A small percentage of implanted cardiac devices, from a well-defined subset, may experience a shortened Recommended Replacement Time (RRT) to End of Service (EOS) interval following an earlier-than-expected RRT observation

Moderate

FDAFeb 3, 2021Nationwide• Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

S-Series Equipment System (Stryker) – Control Interface Issue (2021)

The manufacturer has become aware that there is a likelihood that the S-Series Equipment Management System Capacitive Touch Controls on the MFRs rotational electrical magnetic brakes may disengage when an electrocautery device is in use.

Moderate

FDAJan 29, 2021Nationwide• Stryker Communications

Orient Gene COVID-19 Test (Confirm Biosciences) – Distribution Violation (2021)

Due to two (2) issues: 1) The firm distributed COVID-19 Rapid Test Cassettes outside of the Emergency Use Authorization to non-certified Clinical Laboratories. 2) COVID-19 Rapid Test Cassettes were not adequately validated for its intended use (fingerstick tests for in-home use/testing).

High

FDAJan 29, 2021Nationwide• Confirm Biosciences Inc

Healgen COVID-19 Test (Confirm Biosciences) – Distribution Violation (2021)

High

FDAJan 29, 2021Nationwide• Confirm Biosciences Inc

Anesthesia Gas Machine (Getinge) – CO2 Value Inaccuracy (2021)

Maquet Critical Care AB received complaints where the FiCO2 value was not zero or as close to zero as expected and/or experienced System Check Out failures when docking the absorber to the Flow i Anesthesia machine.

Moderate

FDAJan 29, 2021Nationwide• Getinge Group Logistics America, LLC