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.
3,961 stored notices name Wisconsin, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Wisconsin too — those are in the archive.
Reported Mar 13, 2019
Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Alcon or Endure Ophthalmic Microscope Product Usage: Used for low magnification visualization during ophthalmic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research Laboratories Ltd.
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Phoenix AST-s Indicator, Catalog Number 246009
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Nature's Nectar High Pulp Orange Juice, Never from Concentrate. Item # 420025. Pasteurized. Net 52 FL OZ (1.6 QT)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Citrus Systems Inc.
FDA (openFDA food enforcement)
Reported Mar 6, 2019
Monaco Radiation Treatment Planning (RTP) System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Montmorency Tart Cherry Concentrate 100% Juice 32-oz bottle (sold individual and 12 per case), 16-oz bottle (sold…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.King Orchards
FDA (openFDA food enforcement)
Reported Mar 6, 2019
The WinStation Retinal Imager, also known as Merge Eye Station. DCF-1024 & DCF-512 Digital Imaging System Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Vitality¿ Spinal Fixation System. Thoracolumbosacral pedicle screw system (non-sterile). Pedicle screw fixation is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet Spine Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 27, 2019
AMIA Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 27, 2019
Stingray" Guidewire, labeled as 300cm. intended to facilitate placement of balloon dilatation catheters or other…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Feb 27, 2019
Check-Flo Performer Introducer, Catalog Number RCFW-5.0-25-45-RB-CHB, GPN G11571
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
FDA (openFDA device enforcement)
Reported Feb 20, 2019
COBRA FUSION 50, Ablation System, Catalog # (REF) 700-002
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 20, 2019
Coconut Chocolate RXBARs , 1.83 oz., single bar, , 12-count carton, 5-count carton, 4-count carton
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chicago Bar Company LLC Rxbar
18 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 20, 2019
Hemotherm CE Dual Reservoir Cooler/Heater, Model No. 400CE Product Usage: The HEMOTHERM¿ Model 400CE Dual Reservoir…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cincinnati Sub-Zero Products LLC, a Gentherm Company
FDA (openFDA device enforcement)
Reported Feb 20, 2019
Culinary Secrets, Butterscotch Instant Pudding Mix, Net Wt. 28 OZ, Marketed by Independent Marketing Alliance, Houston,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Diamond Crystal Brands, Inc.
10 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 20, 2019
MOSAIQ¿ Oncology Information System and Sequencer MOSAIQ is an oncology information system used to manage workflows for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Feb 20, 2019
Organic Sunflower Butter, Net Wt. 16 oz. (453g) Packaged under the following brand names: 1. Thrive Market, UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oskri Corp.
19 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 20, 2019
Parent's Choice Toddler Next Stage¿ Milk Drink Powder Natural Milk Flavor With Other Natural Flavors, Stage 3, 1 Year…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PBM Nutritionals, LLC
FDA (openFDA food enforcement)
Reported Feb 20, 2019
The Forest Wild Collection Dark Chocolate bar, CB15052, net wt. 1.25 oz per bar. Product is packaged in a card board…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Salmon River Foods Inc.
FDA (openFDA food enforcement)
Reported Feb 20, 2019
HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Magstim Company Limited
FDA (openFDA device enforcement)
Reported Feb 13, 2019
ARCHITECT Free T3 Reagent Kit used on ARCHITECT i1000SR or i2000/i2000SR platforms Product Usage: It is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 13, 2019
Gold Medal Unbleached All Purpose Flour. Net Wt 5 lb. (2.26kg). UPC 16000-19610. Distributed By General Mills Sales,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.General Mills, Inc.
FDA (openFDA food enforcement)
Reported Feb 13, 2019
Henry Schein CU 1000 Halogen Curing Light, Catalog 900-4542. - Product Usage: Curing light for use in dentistry. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Handpiece Headquarters
FDA (openFDA device enforcement)
Reported Feb 13, 2019
HyVee brand cherry cheese cakes packaged in the following ways: 1) Cheesecake, Net Wt. 8 OZ, HyVee West Des Moines, IA…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hy-Vee Stores Inc.
15 more products in this recall
FDA (openFDA food enforcement)
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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.