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. 2,440 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,440 in last 12 months

Showing 2410124120 of 50,117 recalls

Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 5mm x 40mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 4mm x 80mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 5mm x 40mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2018· Becton Dickinson & Co.

Recalled Item: BD Max Instrument Recalled by Becton Dickinson & Co. Due to A trend for...

The Issue: A trend for false positive Candida glabrata results has been confirmed. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2018· Becton Dickinson & Co.

Recalled Item: BD Max Instrument Reader Spare Part Recalled by Becton Dickinson & Co. Due...

The Issue: A trend for false positive Candida glabrata results has been confirmed. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2018· Roche Diagnostics Corporation

Recalled Item: Roche Diagnostics URISYS 1100 Urine Analyzer Part Number: 03617556001...

The Issue: Limits of Detection (LoD) for protein, nitrite, leukocytes, and erythrocytes...

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

Class II — Potential Health HazardOngoing
DrugSeptember 21, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Nystatin and Triamcinolone Acetonide Cream Recalled by Dr. Reddy's...

The Issue: Failed stability specifications - An out of specification result was...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2018· Teva Pharmaceuticals USA

Recalled Item: Clozapine Orally Disintegrating Tablets Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Disintegration Specifications: Out-of-specification disintegration...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER with Manifold Recalled by The Metrix...

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER with Manifold Recalled by The Metrix...

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: ExactaMix Recalled by The Metrix Company Due to Potential for leaking product

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: ExactaMix Recalled by The Metrix Company Due to Potential for leaking product

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER with Manifold Recalled by The Metrix...

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· DePuy Orthopaedics, Inc.

Recalled Item: CORAIL AMT COXA VARA NECK SEGMENT (KLA) Pro. Code L20432 Recalled by DePuy...

The Issue: There is the potential for debris/material to be found behind the O-rings in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· DePuy Orthopaedics, Inc.

Recalled Item: CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD) Recalled by DePuy...

The Issue: There is the potential for debris/material to be found behind the O-rings in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· DePuy Orthopaedics, Inc.

Recalled Item: CORAIL AMT HIGH OFFSET NECK SEGMENT (KHO) Recalled by DePuy Orthopaedics,...

The Issue: There is the potential for debris/material to be found behind the O-rings in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· Arrow International Inc

Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit Recalled by Arrow International Inc Due to...

The Issue: The products labeling contains inconsistencies. In certain instances, the...

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

Class II — Potential Health HazardOngoing