Product Recalls in Kansas

Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,348 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,348 in last 12 months

Showing 4214142160 of 50,117 recalls

Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2014· Baxter Corporation Englewood

Recalled Item: Abacus 3.1 Recalled by Baxter Corporation Englewood Due to Baxter...

The Issue: Baxter Corporation is initiating a field correction following an upgrade to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2014· Nitinol Devices and Components, Inc.

Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...

The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
FoodMay 27, 2014· Dot Foods Inc.

Recalled Item: Large Pitted Kalamata Olives Recalled by Dot Foods Inc. Due to This...

The Issue: This voluntary recall has been initiated because Savor Brands Large Pitted...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 27, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension¿ Integrated Chemistry Systems intended to measure a variety of...

The Issue: There is a misassembly issue with the photometer installed on Dimension¿...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMay 27, 2014· Vascular Solutions, Inc.

Recalled Item: Langston Dual Lumen Catheters Recalled by Vascular Solutions, Inc. Due to...

The Issue: The inner catheter of some Langston V2 Dual Lumen Catheters have separated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 27, 2014· BioFire Diagnostics, Inc.

Recalled Item: FirmArray Blood Culture Identification (BCID) Panel Recalled by BioFire...

The Issue: BioFire has identified an increased risk of false positive results when the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMay 23, 2014· Dr. Reddy's Laboratories, Inc.

Recalled Item: Dr. Reddy's Metoprolol Succinate Extended Release Tablets Recalled by Dr....

The Issue: Failed Dissolution Specifications: Failure of dissolution test observed at...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodMay 23, 2014· Suntree LLC

Recalled Item: California Grown Shelled Walnuts Recalled by Suntree LLC Due to Potential...

The Issue: Sun Tree is recalling California Grown Shelled Walnuts because they may be...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 23, 2014· Brunkow Cheese of Wisconsin, Inc.

Recalled Item: Fayette Creamery Jalapeno Pepper Raw Milk Cheddar Cold Pack Cheese Recalled...

The Issue: 8 oz tubs of Fayette Creamery brand Jalapeno Raw Milk Cheddar Cold Pack...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Soft-Flow Extended Aortic Cannulae 7.0mm & 8.0mm with or Recalled by...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Cardiovascular Systems, Inc.

Recalled Item: CSI Cardiovascular Systems Recalled by Cardiovascular Systems, Inc. Due to...

The Issue: CSI has initiated a recall on the Diamondback 360 Peripheral Orbital...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns D4 Aortic Arch Cannulae 6.0mm Recalled by Terumo Cardiovascular...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae 28/38 Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Two-stage Venous Return Cannulae 32/40 & 36/51 Fr with Recalled by...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Dual-stage Venous Return Cannulae 28/38 Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Flexible Aortic Arch Cannula 8.0mm with luer Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing