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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

1000

Class I (Serious)

127

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 5981–6000 of 25000 recalls

Alphenix 4D CT System (Canon) – Operational Restriction (2022)

CT operation may be restricted by an interlock which is a result of an system error and the CT system may stop operating properly after an attempt to cancel the error message has been initiated.

FDAMay 3, 2022CA, CO, FL +2 more• Canon Medical System, USA, INC.

Nitrofurantoin Capsules (American Health) – Dissolution Failure (2022)

Failed Dissolution Specifications: Nitrofurantoin Capsules recalled due to dissolution failure at 0-time of the repackaged lot. Drug release results were above specification at 0-time.

Class IIILow

FDAMay 3, 2022Nationwide• American Health Packaging

Losartan Potassium & HCTZ Tablets (Preferred Pharmaceuticals) – AZIDO Impurity High (2022)

CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

Class II

1...298 299300301 302...1250

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Moderate

FDAMay 3, 2022CA, FL, IN• Preferred Pharmaceuticals, Inc.

Losartan Potassium & HCTZ Tablets (Preferred Pharmaceuticals) – AZIDO Impurity High (2022)

CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

Class IIModerate

FDAMay 3, 2022CA, FL, IN• Preferred Pharmaceuticals, Inc.

COVID-19 Collection Tray (American Contract) – assembly training (2022)

Affected products were assembled off-site by individuals who may not have been properly trained.

FDAMay 2, 2022IN, MN• American Contract Systems, Inc.

MVASI Bevacizumab (Amgen) – Loose Crimp Defect (2022)

Defective container: loose crimp defect, potential loss of container integrity.

Class IIModerate

FDAMay 2, 2022Nationwide• Amgen, Inc.

Clean Catch Urine Kit (American Contract) – assembly training (2022)

Affected products were assembled off-site by individuals who may not have been properly trained.

FDAMay 2, 2022IN, MN• American Contract Systems, Inc.

Adult Cap-ONE Biteblock (Nihon Kohden) – expiration problem (2022)

Due to products being shipped/distributed to customers after the products expiration date had past.

FDAApr 29, 2022Nationwide• Nihon Kohden America Inc

Bupropion Hydrochloride Tablets (Sun Pharmaceutical) – Foreign Substance (2022)

Presence Of Foreign Substance: Customer complaint for the presence of dark, gritty substance found within the bottle which was determined to be activated carbon from the desiccant canister inside the bottle.

Class IIILow

FDAApr 29, 2022Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

Bupropion Hydrochloride Tablets (Sun Pharmaceutical) – Foreign Substance (2022)

Class IIILow

FDAApr 29, 2022Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

Truffle Valencia Almonds (New Seasons Market) – Foreign Materials (2022)

Potential foreign materials contamination.

Class IIModerate

FDAApr 29, 2022IN, OR, WA• New Seasons Market LLC

Electric Start Pressure Washers (Generac) – Carbon Monoxide Risk (2022)

This recall involves Generac and DR Power brand electric start pressure washers with model numbers DPW3100DEN, DPW3101DEN, DPW3102DEN, G0071320, G0071321, G0071430 and G0071431. The electric start pressure washers have an electric start/stop button for the unit's gasoline-powered engines, as well as a rechargeable battery used to power the button. The model and serial numbers are printed on a label located on the product's frame. Consumers can check specific unit type, model number and serial number location information at www.generac.com/service-support/product-support-lookup. This recall involves only the following Generac and DR Power brand electric start pressure washers: Recalled Pressure Washers Model Number Serial Number Range DR Pressure Washer PRO 3100 DPW3100DEN 3003024185-3004600505 DR Pressure Washer PRO 3100 DPW3101DEN 3003074891-3004603299 DR Pressure Washer PRO 3100 DPW3102DEN 3006177112-3008763507 3125 CON GAS PW ES CARB EPA3 G0071320 3002690991-3005933713 3125 CON GAS PW ES CARB EPA3 G0071321 3003692980-3009910753 3125 CON GAS PW ES SPEEDWASH CARB EPA3 G0071430 3002778837-3005933361 3125 CON GAS PW ES SPEEDWASH CARB EPA3 G0071431 3006132052-3006132052

CPSCApr 28, 2022Nationwide• Generac Power Systems Inc., of Waukesha, Wisconsin

X80 RADiant Therapy System (Xstrahl) – compatibility issue (2022)

There is a potential compatibility issue with the systems and replacement treatment applicators.

FDAApr 27, 2022CA, FL, KY• Xstrahl Limited

HEB Bakery Simply Delicious Cookies (H-E-B) – metal fragments (2022)

potential metal fragments in product

Class IIModerate

FDAApr 27, 2022TX• H-E-B Grocery Company, LP DBA HEB Milk & Culture Plant #80645

GaviLyte-C (Lupin Pharmaceuticals) – Stability Specification (2022)

Failed Stability Specification

Class IIModerate

FDAApr 27, 2022Nationwide• Lupin Pharmaceuticals Inc.

HEB Bakery Two-Bite Brownies (H-E-B) – metal fragments (2022)

potential metal fragments in product

Class IIModerate

FDAApr 27, 2022TX• H-E-B Grocery Company, LP DBA HEB Milk & Culture Plant #80645

TEG 5000 Fibrinogen Reagent (Haemonetics) – reference range (2022)

Due to a shift in the citrated blood reference range for a normal population, the ranges stated in the IFU are changing. If the clinician relies solely on affected results in comparison to the normal donor reference range, it could lead to misdiagnosis and incorrect treatment or failure to treat.

FDAApr 26, 2022Nationwide• Haemonetics Corporation

1 Series CX Phototherapy (Daavlin) – calibration software issue (2022)

Software issue, resuming an interrupted treatment will result in swap of utilized calibration treatment distance 0" inches to "9. Resulting in over or under dosing.

FDAApr 26, 2022Nationwide• Daavlin Distributing Company

4 Series CX Phototherapy (Daavlin) – calibration software issue (2022)

Software issue, resuming an interrupted treatment will result in swap of utilized calibration treatment distance 0" inches to "9. Resulting in over or under dosing.

FDAApr 26, 2022Nationwide• Daavlin Distributing Company

SE Grocers Cheesecake Sampler (Atlanta Cheesecake) – undeclared pecans (2022)

The firm was notified by a customer that the label does not declare pecans in its ingredient statement.

Class IIModerate

FDAApr 26, 2022FL, LA• Atlanta Cheesecake Company LLC