All recall categories

Recalls distributed in Wisconsin

These notices name Wisconsin in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

3,909 stored notices name Wisconsin, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Wisconsin too — those are in the archive.

Food

Reported Dec 10, 2025

Lava Bun with Green Tea Flavor bright lime green packaging (Frozen) Unsalted butter and cream are listed in the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Prime Food Processing LLC.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 10, 2025

Italian Salad Dressing; Net 1 GAL (3.78L) SKU: 7 67367 00518 4 Creamy Poblano Avocado Ranch Dressing and Dip; Net…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ventura Foods LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 3, 2025

CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K, Description/REF: 25+ TOTALPLUS CP PAK 20K CPM BWV .9 IU/…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alcon Research LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Argon Medical Devices, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Djo, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

FoundationOne CDx (F1CDx), RAL-0003 version 31.0

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Foundation Medicine, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

CareLink Clinic, REF: MMT-7350

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 3, 2025

Nat's Nuts Cinnamon Whiskey Pecans, 4 oz.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nats Nuts LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 3, 2025

Brand Name: Galaxy System Product Name: Galaxy System Model/Catalog Number: GAL-001 Product Description: The Galaxy…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Noah Medical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems Nederland B.v.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Remel, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

REF: CC286297 or BS737162 Automated Digital Cell Morphology analyzer DI-60, IVD in conjunction with a Honeywell Vuquest…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cellavision AB

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

PhD Hemostasis Valve, REF: IN4802/K, IN4802/T, IN4918/A, IN7802/C, IN8802/C, IN9802, IN9802/A, K05-02166B, K05T-02138A,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Merit Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

Brand Name: EZDilate Nephrostomy Balloon Catheter and Inflation Device Kit Product Name: Olympus Nephro-EZDilate…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control materials designed to monitor FOBT (Fecal Occult…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits Model/Catalog Number: 106524US,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Thoratec LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 19, 2025

CEREPAK Detachable Coil System - Name/REF: UNIFORM 2MM X 2.5 CM/FCX100202, UNIFORM 2.5MM X 3.3 CM/FCX100253, UNIFORM…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Cerenovus Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 19, 2025

Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; Product description/Product numbers:…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Medline Industries, LP

20 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 19, 2025

Product Name: Nutra Calm Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 90, Dose: 2 Capsules. Product Sku:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Professional Botanicals, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 19, 2025

Ceiling Type X-Ray Tube Support Models CH-200 and CH-200M used with RADspeed, SonialVision and FLUOROspeed Systems The…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Shimadzu Corporation Medical Systems Division

FDA (openFDA device enforcement)

Medical devices

Reported Nov 19, 2025

Multichem ID-B. Model/Catalog Number: SR103B Intended for use as an unassayed positive qualitative quality control…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Techno-Path Manufacturing Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 12, 2025

Brand Name: Leksell Stereotactic System Product Name: Leksell Vantage Stereotactic System Software Version: n/a Product…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Elekta, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 12, 2025

Strawberry Cheesecake Ice Cream with graham crackers swirl, 12 oz pack, Single Cup Net Wt: 8.75oz, Case of 12…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ice Cream Factory, LLC

1 more product in this recall

FDA (openFDA food enforcement)

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Other states

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.