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. 2,565 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,565 in last 12 months

Showing 1322113240 of 50,117 recalls

DrugFebruary 10, 2022· Positive Health

Recalled Item: RISE UP RED EDITION Capsules Recalled by Positive Health Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 10, 2022· J & M Foods, Inc.

Recalled Item: Favorite Day Carrot cake soft bake cookies Net Wt 8 Recalled by J & M Foods,...

The Issue: Pecans although listed in the Ingredient Statement, was omitted from the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System 3.5 Middle and 3.2 Proximal Saw Recalled...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System Driver SKU: NX-DR Orthopedic surgical...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System 3.5 Middle 3.2 Proximal Kit SKU: Recalled...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System 4.5 Middle 3.2 Proximal Kit SKU: Recalled...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System 4.5 Middle and 3.2 Proximal Saw Recalled...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
DrugFebruary 9, 2022· Walmart Stores

Recalled Item: Avaphinal Maximum Male Enhancement Sexual Pills Recalled by Walmart Stores...

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 9, 2022· Lannett Company, Inc.

Recalled Item: Diazepam Oral Solution (Concentrate) Recalled by Lannett Company, Inc. Due...

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

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 9, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Fructosamine (Fruc) Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Lithium_2 (LITH_2) Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Enzymatic Hemoglobin A1c (A1c_E/A1c_H) Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Calcium_2 (CA_2) Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...

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

Class II — Potential Health HazardOngoing
DrugFebruary 8, 2022· ABC Sales 1 Inc

Recalled Item: MAC DADDY RED Capsules Recalled by ABC Sales 1 Inc Due to Undeclared Tadalafil

The Issue: Marketed Without An Approved NDA/ANDA: product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 8, 2022· Your Favorite Shop

Recalled Item: THE RED PILL Recalled by Your Favorite Shop Due to Undeclared Tadalafil

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 8, 2022· Celebrate Today

Recalled Item: RED MAMMOTH capsules Recalled by Celebrate Today Due to Undeclared Sildenafil

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 8, 2022· ABC Sales 1 Inc

Recalled Item: MAC DADDY PURPLE Capsules Recalled by ABC Sales 1 Inc Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 8, 2022· Bio-Rad Laboratories, Inc.

Recalled Item: BioPlex 2200 SYPH T PACK Syphilis Total & RPR Reagent Pack Recalled by...

The Issue: Due to current concerns related to COVID-19 vaccine interference with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2022· Bio-Rad Laboratories, Inc.

Recalled Item: BioPlex 2200 Syphilis Total & RPR Calibrator Set CAL Recalled by Bio-Rad...

The Issue: Due to current concerns related to COVID-19 vaccine interference with the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 7, 2022· Tsm Brands LLC

Recalled Item: Luxury 70% Isopropyl Alcohol Recalled by Tsm Brands LLC Due to Undeclared Ethyl

The Issue: Labeling - product contains undeclared ethyl alcohol

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

Class II — Potential Health HazardOngoing
Refund