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Ariens Company, of Brillion, Wisconsin

Ariens Company, of Brillion, Wisconsin Recalls

All product recalls associated with Ariens Company, of Brillion, Wisconsin.

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Recall Summary

Total Recalls

1000

Past Year

898

Class I (Serious)

125

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 841–860 of 17592 recalls

Ariens Snow Throwers (Ariens) – Laceration Risk (2025)

Laceration Risk

This recall involves certain Ariens DELUXE-, PLATINUM- and PROFESSIONAL-series Sno-Thro® models. The recalled snow throwers were sold in a bright orange color and are equipped with either rear wheels or tracks. The model and serial numbers are located on the white square ID tag on the frame. Some recalled snowblowers have already been inspected and repaired. Consumers are urged to visit https://www.ariensco.com/safetyrecall for a list of recalled units.

High

CPSCFeb 6, 2025Nationwide• Ariens Company, of Brillion, Wisconsin

Laparoscopy Pack (American Contract) – sterilization uncertainty (2025)

ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.

Moderate

FDAFeb 6, 2025Nationwide• American Contract Systems Inc

Laceration Tray (American Contract) – sterilization uncertainty (2025)

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ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.

Moderate

FDAFeb 6, 2025Nationwide• American Contract Systems Inc

DxI 9000 Analyzer (Beckman Coulter) – interface board issue (2025)

Beckman Coulter identified that an issue for DxI 9000 tip stocker interface (TSI) and reagent storage interface (RSI) boards with the firmware version 1.1.0.0 can cause sub-system communication failures. This failure could result in a delay in reporting patient results.

Moderate

FDAFeb 6, 2025Nationwide• Beckman Coulter, Inc.

Rotarex Atherectomy System (Bard) – catheter breakage (2025)

Atherectomy Catheter eIFU updated to clarify and emphasize procedural steps intended to reduce the likelihood of catheter breakage events. Catheter has an outer cylinder connected to a rotating helix, which could fracture and/or break, which would require retrieval, and helix facture/break could cause vessel injury and lead to severe bleeding.

High

FDAFeb 5, 2025Nationwide• Bard Peripheral Vascular Inc 1625 W 3rd St Bldg 1 850 W. Rio Salado Prkwy. Tempe AZ 85281-2438

DxI 9000 Analyzer (Beckman Coulter) – encoder wheel misalignment (2025)

the DxI 9000 encoder wheel was misaligned on the motor shaft, leading to increased slippage errors and causing the instrument to stop, posing a high safety risk due to potential delays in patient results.

Moderate

FDAFeb 5, 2025Nationwide• Beckman Coulter, Inc.

MEDITECH Expanse Software (Medical Information Technology) – data removal (2025)

Entering multiple keys that trigger input simultaneously may remove data from first field of screens and/or questionnaires with more than one field.

Low

FDAFeb 5, 2025Nationwide• Medical Information Technology, Inc.

Aortic Root Cannula (Medtronic) – luer material issue (2025)

Unexpected loose material in the male luer used in the aortic root cannula has been identified. Potential harms when identified prior to use - procedure delay. Potential harm if not identified and used - stroke (reversible and irreversible).

High

FDAFeb 5, 2025Nationwide• Medtronic Perfusion Systems

Access 2 Analyzer (Beckman Coulter) – sample motor alignment (2025)

Beckman Coulter identified that an issue for Access 2 Sample Motors (B48016) due to improper alignment, causing the motors to rub against the sample wheelbase plate and index sensor. The issue was traced to a worn tool used in production (at the supplier), affecting Access 2 sample motors. This could lead to a potential delay in reporting patient test results.

Moderate

FDAFeb 5, 2025Nationwide• Beckman Coulter, Inc.

IntelePACS Software (Intelerad) – image calculation error (2025)

A software application that receives digital images and data from various sources has a bug in specific software versions that will calculate the Standard Uptake Value (SUV) incorrectly for PET/CT studies acquired on the days of Daylight Savings Time (DST); only on dates in which DST transition occurs; all other dates are unaffected. An incorrect SUV may lead to an incorrect diagnosis.

High

FDAFeb 5, 2025Nationwide• INTELERAD MEDICAL SYSTEMS INCORPORATED 800, Boul. de Maisonneuve Est 12th floor Montreal Canada

Crani Pack (American Contract) – sterilization uncertainty (2025)

During an internal investigation, ACS was unable to confirm that the CODMAN component achieved the required Sterility Assurance Level and therefore is not suitable for sterilization according to ACS procedures.

Moderate

FDAFeb 4, 2025MI• American Contract Systems Inc

VOCSN Ventilators (Ventec) – servicing part issue (2025)

Multi-Function Ventilators were serviced using incorrect parts which have the potential to cause unexpected shutdown, or when using an active circuit could result in inaccurate tidal volume monitor, not triggering on patient efforts, less inspiratory volume, less inspiratory pressure, and less PEEP delivered.

High

FDAFeb 3, 2025CA, IN, MO +1 more• Ventec Life Systems, Inc.

TBS iNsight (Medimaps) – calculation variability (2025)

Potential variability in calculations from fast array scans compared to array scans when operating on Hologic Horizon machines.

Low

FDAFeb 3, 2025AL, AZ, CA +21 more• Medimaps Group Fongit Chemin des Aulx 18 Plan-les-Ouates Switzerland

Access Erythropoietin (Beckman Coulter) – reagent lot variation (2025)

Affected lot (439363) exhibited a negative dose drop of -22% with native patient samples compared to alternate reagent lots. Patient samples tested with the affected lot may demonstrate repeatable falsely decreased results, which may lead to improper diagnosis or repeat testing.

Low

FDAFeb 3, 2025AL, AZ, AR +21 more• Beckman Coulter, Inc.

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.

Moderate

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

Paradigm Insulin Pump MMT-712/715 (Medtronic) – delivery risk (2025)

All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which can be found during airplane take-off or landing. An unexpected additional dose of insulin, which can occur during take-off, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An unexpected under-delivery of insulin, which can occur during landing, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death. During a delivery accuracy dry run testing of the 780G NGP infusion pump under dynamic pressure conditions, the firm observed that when air pressure decreased during take-off simulation, on average 0.569U more insulin was delivered in 15 minutes than the expected delivery volume at ambient pressure at 1 U/hr delivery rate; when air pressure increased during landing simulation, on average 0.537 U less insulin was delivered in 25 minutes than the expected delivery volume at ambient pressure at 1 U/hr delivery rate. The firm also observed that the mechanisms causing the variations in delivery volumes are independent of the delivery rate.

Very High

FDAJan 31, 2025Nationwide• Medtronic MiniMed, Inc.

Stay Informed

Ariens Company, of Brillion, Wisconsin Recalls

Recall Summary

Ariens Snow Throwers (Ariens) – Laceration Risk (2025)

Laparoscopy Pack (American Contract) – sterilization uncertainty (2025)

Laceration Tray (American Contract) – sterilization uncertainty (2025)

DxI 9000 Analyzer (Beckman Coulter) – interface board issue (2025)

Rotarex Atherectomy System (Bard) – catheter breakage (2025)

DxI 9000 Analyzer (Beckman Coulter) – encoder wheel misalignment (2025)

MEDITECH Expanse Software (Medical Information Technology) – data removal (2025)

Aortic Root Cannula (Medtronic) – luer material issue (2025)

Access 2 Analyzer (Beckman Coulter) – sample motor alignment (2025)

IntelePACS Software (Intelerad) – image calculation error (2025)

Crani Pack (American Contract) – sterilization uncertainty (2025)

VOCSN Ventilators (Ventec) – servicing part issue (2025)

TBS iNsight (Medimaps) – calculation variability (2025)

Access Erythropoietin (Beckman Coulter) – reagent lot variation (2025)

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

Paradigm Insulin Pump MMT-712/715 (Medtronic) – delivery risk (2025)

MiniMed 640G Insulin Pump (Medtronic) – delivery risk (2025)

Brivo MR355 MRI System (GE Healthcare) – SAR monitoring (2025)

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

MiniMed 670G Insulin Pump (Medtronic) – delivery risk (2025)