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. 2,741 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,741 in last 12 months

Showing 2140 of 52,482 recalls

FoodFebruary 6, 2026· Valley Springs Artesian Gold, LLC

Recalled Item: Valley Springs 100% Natural Bottled Water packaged in the following Recalled...

The Issue: Water was bottled under insanitary conditions.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 6, 2026· Trividia Health, Inc.

Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...

The Issue: The system labeling (user manual and online labeling) did not provide...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 6, 2026· International Life Sciences

Recalled Item: Artelon FlexBand Dynamic Matrix Recalled by International Life Sciences Due...

The Issue: Augmentation devices failed bacterial endotoxin testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2026· Trividia Health, Inc.

Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...

The Issue: The system labeling (user manual and online labeling) did not provide...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 6, 2026· Trividia Health, Inc.

Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...

The Issue: The system labeling (user manual and online labeling) did not provide...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 6, 2026· International Life Sciences

Recalled Item: Artelon FLEXBAND TWIST .12 3.85x17mm HEX Anchor (Qty Recalled by...

The Issue: Augmentation devices failed bacterial endotoxin testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2026· International Life Sciences

Recalled Item: Artelon FlexBand Plus & 41057 Recalled by International Life Sciences Due to...

The Issue: Augmentation devices failed bacterial endotoxin testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2026· Trividia Health, Inc.

Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...

The Issue: The system labeling (user manual and online labeling) did not provide...

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

Class I — Serious Health HazardOngoing
DrugFebruary 5, 2026· Fresenius Kabi Compounding, LLC

Recalled Item: thiamine HCl Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 5, 2026· Fresenius Kabi Compounding, LLC

Recalled Item: ketamine HCl Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 5, 2026· Fresenius Kabi Compounding, LLC

Recalled Item: vancomycin HCl Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 5, 2026· Fresenius Kabi Compounding, LLC

Recalled Item: vancomycin HCl Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 5, 2026· Fresenius Kabi Compounding, LLC

Recalled Item: acyclovir sodium Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 5, 2026· Remel, Inc

Recalled Item: Campy CVA Medium 100/PK Recalled by Remel, Inc Due to Customer complaints...

The Issue: Customer complaints report low to no recovery of Campylobacter Jejuni ATCC...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2026· Diagnostica Stago, Inc.

Recalled Item: Brand Name: STA Liatest Free Protein S Product Name: STA Recalled by...

The Issue: The potential of out-of-range results and an underestimation of the free...

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

Class II — Potential Health HazardOngoing
FoodFebruary 3, 2026· Prime Food Processing LLC.

Recalled Item: Prime Food Processing Dried Croaker Fish Recalled by Prime Food Processing...

The Issue: Uneviscerated Fish

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 3, 2026· Pure Solutions, Inc.

Recalled Item: Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep...

The Issue: Label declares bovine colostrum but does not declare milk allergen.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 3, 2026· Exactech, Inc.

Recalled Item: Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle...

The Issue: Impactor handle may be missing cross-pin

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2026· Exactech, Inc.

Recalled Item: Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit...

The Issue: Impactor handle may be missing cross-pin

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2026· Ion Beam Applications S.A.

Recalled Item: IBA Proton Therapy System - PROTEUS 235 Recalled by Ion Beam Applications...

The Issue: It was identified that eh Universal Beam Triggering Interface (UBTI) is...

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

Class II — Potential Health HazardOngoing