Product Recalls in Wisconsin

Product recalls affecting Wisconsin — including food, drugs, consumer products, medical devices, and vehicles distributed to Wisconsin. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,736 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,736 in last 12 months

Showing 31213140 of 52,482 recalls

FoodFebruary 15, 2025· ZB Importing LLC

Recalled Item: Ulker Kekstra Mini strawberry Recalled by ZB Importing LLC Due to Milk not...

The Issue: Milk not declared as the major food allergen source for the ingredient Whey

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2025· ZB Importing LLC

Recalled Item: Ulker Dankek Roll Cake Banana Recalled by ZB Importing LLC Due to Wheat not...

The Issue: Wheat not listed in Contains statement

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2025· ZB Importing LLC

Recalled Item: Ulker Biskrem Cocoa Biscuit Recalled by ZB Importing LLC Due to Undeclared Wheat

The Issue: Undeclared wheat and egg

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 15, 2025· ZB Importing LLC

Recalled Item: Ulker Rulokat Hazelnut Wafers Recalled by ZB Importing LLC Due to Undeclared Egg

The Issue: Undeclared egg

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 15, 2025· Abbott Medical

Recalled Item: Aveir DR Leadless Pacemaker (LP) Ventricular Device UDI-DI Recalled by...

The Issue: Due to a manufacturing issue, leadless pacemakers may have been exposed to...

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

Class II — Potential Health HazardOngoing
DrugFebruary 14, 2025· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Clear 1mL Applicators Recalled by CareFusion 213, LLC Due to...

The Issue: Non-Sterility: contamination of Aspergillus penicillioides, due to breach in...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 14, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: A problem was discovered during the scanning process of the outer carton...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2025· Smiths Medical ASD, Inc.

Recalled Item: CAPNOCHECK BCI Airway Adapter Recalled by Smiths Medical ASD, Inc. Due to...

The Issue: Airway adapter does not meet specification and may break off when attaching...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: A problem was discovered during the scanning process of the outer carton...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2025· Smiths Medical ASD, Inc.

Recalled Item: CAPNOCHECK BCI Airway Adapter Recalled by Smiths Medical ASD, Inc. Due to...

The Issue: Airway adapter does not meet specification and may break off when attaching...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: A problem was discovered during the scanning process of the outer carton...

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

Class II — Potential Health HazardOngoing
DrugFebruary 13, 2025· Johnson, S C and Son, Inc

Recalled Item: Kids by babyganics SPF 50 mineral sunscreen totally tropical (titanium...

The Issue: Chemical Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 13, 2025· ICU Medical, Inc.

Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by ICU Medical, Inc. Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength. Overwrap labeled as Potassium...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 13, 2025· ICU Medical, Inc.

Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by ICU Medical, Inc. Due to Mislabeling

The Issue: Labeling: Label Error on Declared Strength. Cases labeled POTASSIUM CHLORIDE...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 13, 2025· Johnson, S C and Son, Inc

Recalled Item: Kids by babyganics SPF 50 totally tropical (titanium dioxide 3/5% Recalled...

The Issue: Chemical Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 13, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Nelarabine Injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 13, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Nelarabine Injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 13, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Proxima Drape labeled as PACK Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Potential breach in pouch packaging which could lead to loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Proxima Drape labeled as ORTHO TRAUMA CDS Recalled by MEDLINE INDUSTRIES, LP...

The Issue: Potential breach in pouch packaging which could lead to loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Proxima Drape labeled as UNIVERSAL DAVINCI ROBOTIC P. Sterile surgical...

The Issue: Potential breach in pouch packaging which could lead to loss of sterility.

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

Class II — Potential Health HazardOngoing