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.

Medical devices

Reported Feb 25, 2026

MONARCH Platform, Bronchoscopy, Catalog Numbers: MON-000005-01 , MON-000005-01R , MON-000006 , MON-000006-RFB,…

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

Auris Health, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 25, 2026

Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 25, 2026

Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset, Net Wt., 1 fl oz (30 ml) liquid…

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

Pure Solutions, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 25, 2026

MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marker UDI (GTIN):…

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

Stryker Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 18, 2026

Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11.1 Product…

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

Elekta, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 18, 2026

da Vinci 5 Surgeon Console Viewer Display, ASSY, DV5 CONSOLE, IS5000, Part Number: 380730-45

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 18, 2026

Ore-Ida Tater Tots shaped potatoes, item number OIF00215A. Frozen potato product is packaged in clear unlabeled poly…

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

McCain Foods USA Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 18, 2026

Spicy Breakfast Burrito in a flour tortilla. Net Weight 10 oz (283g) Scrambled eggs, Salsa, Potatoes, Jalapenos,…

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

MG Foods-Compass Group

FDA (openFDA food enforcement)

Food

Reported Feb 18, 2026

CREAMY PEANUT BUTTER NET WT 0.75 OZ(21g) DISTRIBUTED BY US FOODS, ROSEMONT, IL 60018; PEANUT BUTTER NET WT. 0.5OZ & NET…

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

Ventura Foods LLC

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 11, 2026

Repackaged M&Ms Peanut candies, Net Wt 1.3 oz. Item BB471BG. Labeled as Make Your Mark. For nutrition facts information…

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

Beacon Promotions Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 11, 2026

COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in…

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

Beckman Coulter, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 11, 2026

FDR Visionary Suite; Model Number: CH-200; Version: (1) 566-16130-23, (2) 566-16130-31, (3)

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

FUJIFILM Healthcare Americas Corporation

FDA (openFDA device enforcement)

Food

Reported Feb 11, 2026

Imu-Tek Immuno-5 Colostrum Powder 7 oz. Intended Use: Dietary Supplement for People. (Some customers use this for their…

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

Imu-Tek Animal Health, Incorporated

FDA (openFDA food enforcement)

Medical devices

Reported Feb 11, 2026

Brand Name: Da Vinci Product Name: da Vinci X, Xi Surgical System, & da Vinci 5 Surgical System Model/Catalog Number:…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 11, 2026

MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software Version 6.60 The MiniMed 780G insulin pump…

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 11, 2026

Bread Crumbs, Outside The Breadbox brand, net wt. 8 oz, UPC 873799001554. Product is packaged in a clear stand up…

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

Vh Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 11, 2026

Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens, Catalog VFD 2. Volk Magnifying Lens, Catalog VMD

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

Vortex Surgical Inc.

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 4, 2026

BEAR Implant. Model Number: 1000.

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

Miach Orthopaedics

FDA (openFDA device enforcement)

Food

Reported Feb 4, 2026

Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count bottle, BIO7772 120 count…

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

Quten Research Institiute LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 4, 2026

Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R; Siemens Material Number (SMN): 11574002; With Software…

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

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 28, 2026

The LDL-Cholesterol assay is comprised of two distinct phases. In phase one a unique detergent solubilizes cholesterol…

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

Beckman Coulter Ireland, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 28, 2026

Gregory's Foods Bag Full of Cookies, White Chocolate Macadamia Nut, frozen cookie dough. Net Wt 2 lbs 8.5 oz (1148g).…

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

Gregory's Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 28, 2026

Tego Connector: REF: 011-D1000, 01C-D1000, 055-D1000, D1000; Conector Tego: REF: LAT-D1000

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

ICU Medical, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 28, 2026

Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Bag Model/Catalog Number: 490127 Software Version:…

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

Intuitive Surgical, Inc.

FDA (openFDA device 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.