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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 48,122 notices were distributed nationwide, so they reach Wisconsin too — those are in the archive.

Medical devices

Reported Jun 15, 2016

GE Revolution CT The system is intended for head, whole body, cardiac and vascular X-ray Computed Tomography…

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

GE Healthcare, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 15, 2016

Karlsburger, Mesquite Seasoning Mix & Marinade, Item 46402, Net WT 2 lbs in plastic shaker jars.

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

Karlsburger Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 15, 2016

Sedecal SA Mobile Diagnost w DR x-ray system

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

Sedecal USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 15, 2016

Maestro Air Motor Pneumatic cranial drill motor. The Maestro Air Pneumatic System is a pneumatically operated surgical…

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

Stryker Instruments Div.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 15, 2016

Persona Trabecular Metal Tibia; Persona Trabecular Metal Tibial Plate Instruments and Modular Brackets; Used to…

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

Zimmer Biomet, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2016

The ARCHITECT Estradiol Kit Intended to measure estradiol, an estrogenic steroid, in plasma.

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

Abbott Laboratories

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2016

Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite Valve Product Usage: Used for aspiration of…

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

B. Braun Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2016

Monaco RTP System Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2016

Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments

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

Integra LifeSciences Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 8, 2016

Angel Wings Complete Daily Multi with 146 nutrients including Anti-aging and Superfruit Antioxidants and 75 Plant…

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

Liquid Assets Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 8, 2016

Replacement HEPA filter for Natus Sterile-Drier Model 43 and Model 44. Filter Catalogue Part Number: 54343, 54344, and…

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

Natus Medical Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2016

Dimension Vista 500 Intelligent Lab System running on software versions V.3.6.1 SP1 or V.3.6.2, Device listing #…

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

Siemens Healthcare Diagnostics Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2016

EZ Slide Battery/line powered hydraulic table with removable leg section and 21 top slide General Purpose Surgical…

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

Skytron, Div. The KMW Group, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2016

Reprocessed Microline Scissor Tips intended to be used with a reusable hand piece and designed for minimally invasive…

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

Sterilmed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2016

STAT-Check Resuscitation Bag Manual Emergency Resuscitation Bag with Carbon dioxide gas analyzer Intended for use in…

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

Ventlab LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2016

GE Healthcare, Discovery IGS 730. Indicated for use in generating fluoroscopic and rotational images of human anatomy.

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

GE Medical Systems, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 1, 2016

Mighty Leaf Tea Company Organic Ginger Peach Iced Tea; 100/1 oz. per case Item number 60001. UPC: 00656252600019

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

Mighty Leaf Tea

FDA (openFDA food enforcement)

Medical devices

Reported Jun 1, 2016

3.2 mm Three-fluted drill bit, sterile, Catalog ID # 03.010.060S Product Usage: Usage: The 3.2 mm Three-fluted Drill…

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

Synthes (USA) Products LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 25, 2016

Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and…

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

Diamedix Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 25, 2016

Colby Jack cheese, 8 oz. and 16 oz, Vacuumed plastic pouches

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

Msu Dept Of Fd Sci Dairy Plant

FDA (openFDA food enforcement)

Food

Reported May 25, 2016

Sugarfina Chocolate Malt Balls UPC Code 840278113565 SKU K1159

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

Sugarfina, LLC

FDA (openFDA food enforcement)

Food

Reported May 25, 2016

COMMERCIAL WHEAT GERM 274000, 50.00 lbs. (22.68 kg); UPC Code: 0-26938-46535-3

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

Unfi

FDA (openFDA food enforcement)

Medical devices

Reported May 18, 2016

Direct Drive Clip Applier CA090, indicated for ligation of tubular structures or vessels in laparoscopic and general…

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

Applied Medical Resources Corp.

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2016

Ascom Mobile Monitoring Gateway (versions 4.1.1 and 4.2.0) and Ascom Unite Connect for Nurse Call (version 2.2.0).

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

Ascom US, 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.