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. 2,386 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,386 in last 12 months

Showing 3812138140 of 50,117 recalls

FoodMay 22, 2015· Vitamin Cottage Natural Food Markets, Inc.

Recalled Item: Natural Grocers Raw Macadamia Nuts Recalled by Vitamin Cottage Natural Food...

The Issue: Vitamin Cottage Natural Food Markets Inc. is recalling various lots of...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 22, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Divalproex Sodium Extended-Release Tablets Recalled by Dr. Reddy's...

The Issue: Failed Dissolution Specifications; exceeded specification at the 9 hour time...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Divalproex Sodium Extended-Release Tablets Recalled by Dr. Reddy's...

The Issue: Failed Dissolution Specifications; exceeded specification at the 9 hour time...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 21, 2015· Medtech Products, Inc.

Recalled Item: SUCRETS Sore Throat & Cough Vapor Cherry lozenges Recalled by Medtech...

The Issue: Labeling: Label Mix-Up: An incorrect book label for Sucrets Sore Throat,...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 21, 2015· Takeda Pharmaceuticals North America, Inc.

Recalled Item: CONTRAVE (naltrexone HCl and bupropion HCl )extended-release tablets...

The Issue: Failed Tablet/Capsule Specifications: Potential tablet defect of broken...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 21, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Healthcare Diagnostics Dimension Vista Systems Recalled by Siemens...

The Issue: Two software issues may occur in Vista software version 3.6.1. Issue #1:...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2015· Exactech, Inc.

Recalled Item: Exactech Ambassador Cervical Plate System The Exactech Ambassador Cervical...

The Issue: Shipped to a single consignee prior to completion of final inspection.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2015· Exactech, Inc.

Recalled Item: Exactech Single Barrel Drill Guides The Single Barrel Drill Guide Recalled...

The Issue: Shipped to a single consignee prior to completion of final inspection.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2015· Elekta, Inc.

Recalled Item: Oncentra Brachy radiation therapy planning software designed to analyze and...

The Issue: Incorrect dose calculation for Regions of Interest (ROIs) defined on a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2015· Fresenius Medical Care Holdings, Inc.

Recalled Item: NaturaLyte Liquid Bicarbonate Concentrate (Dialysate Concentrate for...

The Issue: Bacterial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2015· Northern Digital Inc.

Recalled Item: NDI Disposable Marker Spheres for Brainlab IGS (Image Guided Recalled by...

The Issue: Inadequate curing of adhesive, which may cause the two halves of the spheres...

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

Class II — Potential Health HazardOngoing
DrugMay 20, 2015· Mylan Lab Inc

Recalled Item: Mycophenolic Acid Delayed-release Tablets Recalled by Mylan Lab Inc Due to...

The Issue: Failed Dissolution Specifications: Low out of specification dissolution results.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 19, 2015· Hospira Inc.

Recalled Item: Magnesium Sulfate Injection Recalled by Hospira Inc. Due to Failed pH...

The Issue: Failed pH Specifications: 12 month stability testing

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 19, 2015· Pointe Scientific, Inc.

Recalled Item: Pointe Scientific G6PD Controls Kit configuration: 6 x 0.5 ml Recalled by...

The Issue: A reduction in the reconstituted stability has been identified. Clinicians...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2015· Remel Inc

Recalled Item: VersaTREK Instrument Series 528 Recalled by Remel Inc Due to Use of the...

The Issue: Use of the recalled product may result in false positive reports.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2015· Remel Inc

Recalled Item: VersaTREK Instrument Series 240 Recalled by Remel Inc Due to Use of the...

The Issue: Use of the recalled product may result in false positive reports.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: CentraLink" Data Management System Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has determined that the sample query function...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Tni-Ultra Assay Recalled by Siemens Healthcare Diagnostics,...

The Issue: System-to-system bias between the Tni-Ultra assay on the ADVIA Centaur CP...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2015· Zimmer, Inc.

Recalled Item: M/L Taper with Kinectiv¿ Technology. prosthesis Recalled by Zimmer, Inc. Due...

The Issue: Zimmer is initiating a voluntary recall of 64 lots (752 implants total) of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 18, 2015· Edwards Lifesciences, LLC

Recalled Item: ClearSight Recalled by Edwards Lifesciences, LLC Due to Edward Lifesciences...

The Issue: Edward Lifesciences is recalling the ClearSight System because the finger...

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

Class II — Potential Health HazardOngoing