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Barco N.V. President Kennedypark 35 Kortrijk Belgium

Barco N.V. President Kennedypark 35 Kortrijk Belgium Recalls

All product recalls associated with Barco N.V. President Kennedypark 35 Kortrijk Belgium.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 4561–4580 of 37665 recalls

Barco MDSC Flowcell (Barco) – cable manufacturing problem (2023)

Barco became aware of a problem with I2C cables in the manufacturing process of a limited batch of MDSC-85xx NXF products. The functionality of the built-in MNA decoder is blocked.

Moderate

FDADec 20, 2023Nationwide• Barco N.V. President Kennedypark 35 Kortrijk Belgium

Medline Bleach Wipes (Medline) – shelf life concern (2023)

There is stability concern for products dated with a 24-month shelf life. Product is safe and effective up to 12 months shelf life.

Low

FDADec 20, 2023Nationwide• MEDLINE INDUSTRIES, LP Northfield

Medfusion 3500 Pump (Smiths Medical) – software alarm issue (2023)

Medfusion syringe pumps, with software versions before v6.0.0, may have the following issues:1. Delivery During Motor Not Running High Priority Alarm, 2. Infusion Restarted with Incorrect Parameters, 3. Screen Lock, 4. Interruption of Bolus or Loading Dose Delivery, 5. Pump Displays Incorrect Bolus/Loading Dose, 6. Loading/Bolus Dose Below the Minimum Recommended Rate, 7. Motor Rate Error, 8. Incorrect Recall Last Settings, 9. Corrupt Configuration, 10. Auto Lock, 11. Toolbox Configuration Loading Dose Time Values. Smiths Medical corrected all issues included in this notification in previous software updates and the corrections were carried forward into all subsequent software releases. Please ensure you have the most recent Medfusion software (v6.0.0) installed on your pumps.

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High

FDADec 19, 2023Nationwide• Smiths Medical ASD Inc.

Medfusion Barrel Clamp (Smiths Medical) – pump component risk (2023)

Medfusion Model 4000, 3500, and 3010 pumps manufactured or serviced with Barrel Clamp Guide (Part Number G6000716), Lot Numbers P0407365, P0486670, and P0561740 may contain a molding defect that could potentially lead to slippage of the spring within the barrel clamp assembly. If this occurs, it could result in the inability of the pump to recognize a syringe or the pump may misidentify the size of the syringe loaded.

Moderate

FDADec 19, 2023Nationwide• Smiths Medical ASD Inc.

Medfusion 4000 Pump (Smiths Medical) – software alarm issue (2023)

Medfusion Model 4000 syringe infusion pumps, with the following software versions, may have the following issues: 1. Delivery During Motor Not Running High Priority Alarm (v1.0.0, v1.1.0, v1.1.1, v1.1.2), 2. Re-administered Loading Dose (v1.0.0, v1.1.0, v1.1.1, v1.1.2), 3. Incorrect Critical Data Failure Alarm, 4. Interruption of Bolus or Loading Dose Delivery (v1.0.0, v1.1.0, v1.1.1, v1.1.2), 5. Incorrect Total Bolus/Loading Dose Displayed (v1.1.0, v1.1.1, v1.1.2), 6. Volume Limit Before Bolus/Loading Dose Complete (v1.1.2), 7. Drug Library Lower Limit Displayed Incorrectly (v1.6.0, v1.6.1), 8. Depleted Battery Alarm (All versions previous to v1.6.5), 9. Loss of Wireless Connectivity (v1.5.0, v1.5.1, v1.6.0, v1.6.1, v1.6.4), 10. PharmGuard Server Password (v2.3, v2.4, v2.5). Smiths Medical corrected all issues included in this notification in previous software updates and the corrections were carried forward into all subsequent software releases. Please ensure you have the most recent Medfusion software installed on your pumps.

High

FDADec 19, 2023Nationwide• Smiths Medical ASD Inc.

Syringe Pumps (Smiths Medical) – Barrel Clamp Guide Defect (2023)

Moderate

FDADec 19, 2023Nationwide• Smiths Medical ASD Inc.

Medfusion Syringe Pumps (Smiths Medical) – Barrel Clamp Guide Defect (2023)

Moderate

FDADec 19, 2023Nationwide• Smiths Medical ASD Inc.

iQ200 Urine Analyzers (Beckman Coulter) – Cannula Rust Risk (2023)

Beckman Coulter has become aware that the cannula, which is found in the Flowcell and the iQClear Rinse Waste Well Assembly, may rust. Rust from the cannula has the potential to generate erroneous results.

Moderate

FDADec 19, 2023Nationwide• Beckman Coulter, Inc.

EndoVive Button Kit (Boston Scientific) – measurement error (2023)

Affected batches of the kit contain Stoma Measuring Devices sized to measure for an 18/24F replacement button, but are labeled as being for a 28F. Use of defective product may lead to undersizing the button, which may cause embedding with erosion into the gastric wall, tissue necrosis, infection, sepsis, and associate sequelae.

High

FDADec 19, 2023Nationwide• Boston Scientific Corporation

REV 2 Flowcell (Beckman Coulter) – cannula rust problem (2023)

Moderate

FDADec 19, 2023Nationwide• Beckman Coulter, Inc.

Basecamp Travel Trailer (Airstream) – Spare Tire Bracket Fatigue (2023)

Airstream, Inc. (Airstream) is recalling certain 2012-2023 Basecamp 20X travel trailers. The spare tire carrier bracket may experience metal fatigue and break, allowing the spare tire to detach from the trailer.

High

NHTSADec 19, 2023Nationwide• AIRSTREAM

Intellis Programmer (Medtronic) – Session Establishment Issue (2023)

Medtronic has discovered an instance in which the Intellis A710 Clinician Programmer Application (CP App) could no longer establish a session with the Implantable Neurostimulator (INS) which resulted in the inability for the clinician to adjust stimulation parameters. In the event of this issue, the patient may receive inadequate or excessive therapy and experience non-optimal pain relief.

High

FDADec 19, 2023Nationwide• Medtronic Neuromodulation

iQ Waste Well Adapter (Beckman Coulter) – Cannula Rust Risk (2023)

Moderate

FDADec 19, 2023Nationwide• Beckman Coulter, Inc.

DxU Microscopy Analyzers (Beckman Coulter) – Cannula Rust Risk (2023)

Moderate

FDADec 19, 2023Nationwide• Beckman Coulter, Inc.

Tesla Model S (Tesla) – Door Unlock Risk (2023)

Tesla, Inc. (Tesla) is recalling certain 2021-2023 Model S and X vehicles. The cabin doors can be unlocked during a crash. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 214, "Side Impact Protection."

High

NHTSADec 19, 2023Nationwide• TESLA

Portable Power Generator (Doosan) – Brake Harness Problem (2023)

Doosan Portable Power (Doosan) is recalling certain 2019-2023 Portable Generator Trailers. The electric brake harness was connected to the battery disconnect switch instead of the positive distribution lug of the battery, deenergizing the brakes when the battery disconnect switch is in the off position.

High

NHTSADec 19, 2023Nationwide• DOOSAN PORTABLE POWER

Cheddar Kettle Corn (Sweet and Simple) - Undeclared Ingredients (2023)

Cheddar Popcorn label does not declare milk or sub-ingredients, Maltodextrin, Sunflower oil, Yellow #5, Yellow #6, and Lactic Acid.

Class IIModerate

FDADec 19, 2023IN, MO• Sweet and Simple Kettle Corn

TactiFlex Ablation Catheter (St. Jude) – System Recognition Issue (2023)

When the catheters are used with the EnSiteX EP System, the system does not correctly recognize the catheter as the appropriate product model and instead reads and displays it as a different model. This results in some features specific to the catheter do not appear on the display and the catheter image may also appear inverted.

High

FDADec 18, 2023Nationwide• St. Jude Medical, Atrial Fibrillation Division, Inc.

ACTU8 Forceps (Vortex Surgical) – Residue Contamination (2023)

Reason for the voluntary recall is residue was identified on the two forceps tips of a customer in Korea. The residue is associated with one lot of forceps tips which were utilized in two lots of ACTU8 Adaptive Forceps Tips occurring in 0.25% of those lots.

Moderate

FDADec 18, 2023Nationwide• Vortex Surgical Inc.

Aldi Choceur Chocolate Bars (Astor) - Undeclared Coconut (2023)

Undeclared Allergen

Undeclared coconut

Class IIModerate

FDADec 18, 2023FL, IN• Astor Chocolate Corp.