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. 2,451 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,451 in last 12 months

Showing 2274122760 of 50,117 recalls

DrugApril 5, 2019· Brian P. Richardson

Recalled Item: Kopi Jantan Tradisional Natural Herbs Coffee Recalled by Brian P. Richardson...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 5, 2019· Abbott Gmbh & Co. KG

Recalled Item: Alinity i Processing Module Recalled by Abbott Gmbh & Co. KG Due to...

The Issue: Potential loose cable connections on the reagent cooler, which could result...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2019· Advanced Bionics, LLC

Recalled Item: SoundWave Professional Suite Software 3.2 Recalled by Advanced Bionics, LLC...

The Issue: The manufacturer received complaints that customers were attempting to...

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

Class III — Low RiskOngoing
Medical DeviceApril 4, 2019· Roche Diagnostics Corporation

Recalled Item: cobas p 701 post-analytical units Recalled by Roche Diagnostics Corporation...

The Issue: There is a potential for the tray input flap on the post analytical units to...

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

Class III — Low RiskOngoing
Medical DeviceApril 4, 2019· Roche Diagnostics Corporation

Recalled Item: cobas p 501 post-analytical units Recalled by Roche Diagnostics Corporation...

The Issue: There is a potential for the tray input flap on the post analytical units to...

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

Class III — Low RiskOngoing
Medical DeviceApril 3, 2019· Becton Dickinson & Co.

Recalled Item: BD Veritor System Reader -In Vitro Diagnostic for use with Recalled by...

The Issue: Background calibration has the potential to cause false positive or false...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2019· Thommen Medical AG

Recalled Item: Adapter for handpiece Recalled by Thommen Medical AG Due to Dental adaptor...

The Issue: Dental adaptor does not conform to specifications. The dental coupling of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2019· Bio-Rad Labs

Recalled Item: Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test Recalled by...

The Issue: An elevated lot-to-lot bias was observed for Autoimmune EIA Anti-Tissue...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2019· Becton Dickinson & Co.

Recalled Item: BD Veritor Plus Analyzer- In-Vitro Diagnostic intended to use with Recalled...

The Issue: Background calibration has the potential to cause false positive or false...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2019· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: 2008T BlueStar Machine Software v.2.72-Hemodialysis machine Model Number:...

The Issue: Power Logic Board Fail Message on the 2008T BlueStar Machine with software...

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

Class III — Low RiskOngoing
Medical DeviceApril 3, 2019· Elekta Limited

Recalled Item: Elekta Unity systems Product Usage: Elekta Unity using Magnetic Resonance...

The Issue: There is no warning in the Elekta Unity manual for the administration of...

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

Class II — Potential Health HazardOngoing
FoodApril 3, 2019· ConAgra Foods, INc.

Recalled Item: Hunts Tomato Paste No Salt Added 6 ounce cans Recalled by ConAgra Foods,...

The Issue: Mold. This situation is due to potential damage to the cans.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Methionine 15mg/Choline 100mg/ Inositol 50mg/ Methylcobalamin 1mg/...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Sermorelin 0.4 mg/0.5 mL Recalled by Anderson Compounding Pharmacy, Inc. DBA...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Prostaglandin 20 mcg/mL Recalled by Anderson Compounding Pharmacy, Inc. DBA...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: HCG 20 Day Injection Recalled by Anderson Compounding Pharmacy, Inc. DBA...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: DMSO 50% 60 mL/Heparin 1 mL/ Sodium Bicarbonate 60 mL/ Solu-Cortef 100 mg...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Heparin 10 mL/ Marcain 0.25% 20 mL/Sodium Bicarbonate 8.4%-40 mL/ Recalled...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Heparin 20 Recalled by Anderson Compounding Pharmacy, Inc. DBA Anderson...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Sermorelin 0.3 mg/0.5 mL Recalled by Anderson Compounding Pharmacy, Inc. DBA...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund