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. 1,785 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,785 in last 12 months

Showing 3480134820 of 50,117 recalls

Medical DeviceFebruary 17, 2016· Applied Medical Technology Inc

Recalled Item: Wilson Implantation System Product Usage: Indicated to aid in tissue...

The Issue: The firm received a complaint of an open pouch which breaches the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: Universal Quick Adjust under the following labels: 1) Aluminum crutch...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

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

Class II — Potential Health HazardOngoing
FoodFebruary 17, 2016· Reily Foods Co.

Recalled Item: CARROLL SHELBY'S(R) ORIGINAL TEXAS BRAND White CHICKEN CHILI KIT Recalled by...

The Issue: Cartons of Carroll Shelby White Chicken Chili (3oz retail carton) produced...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Genzyme Corporation

Recalled Item: Thyrogen (thyrotropin alfa for injection) Recalled by Genzyme Corporation...

The Issue: Presence of Particulate Matter: Glass particles found in the product after...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Actavis Elizabeth LLC

Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Actavis Elizabeth LLC

Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Actavis Elizabeth LLC

Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Actavis Elizabeth LLC

Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Genzyme Corporation

Recalled Item: Thyrogen (thyrotropin alfa for injection) Recalled by Genzyme Corporation...

The Issue: Presence of Particulate Matter: Glass particles found in the product after...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 6.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Biomet, Inc.

Recalled Item: Verso Shoulder Forked Retractor (Comprehensive Instrumentation 2 Prong...

The Issue: Zimmer Biomet Inc. Verso Shoulder Forked Retractor (Comprehensive...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 4.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 4.5 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes Interlocking Bolt Recalled by Synthes (USA) Products LLC Due to...

The Issue: DePuy Synthes is initiating a voluntary medical device recall of certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 7.0 mm and 7.3 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 6.5 mm Cancellous Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: CIOS ALPHA (Image-intensified fluoroscope x-ray system) Product Usage: The...

The Issue: Siemens found a defective part in their production line which could increase...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 3.5 mm and 4.0 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 4.0 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing