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.

Food

Reported Jul 24, 2019

Wilton Chocolate decorator icing stiff consistency 16 oz plastic tub retail unit 6 or 12 retail units per wholesale unit

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

Wilton Brands

FDA (openFDA food enforcement)

Medical devices

Reported Jul 17, 2019

Alaris Pump Infusion Set, Model Codes 10010453, 10010454, 10012144, 10015294, 10015414, 10933805, 11171447, 11404930,…

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Jul 17, 2019

Radrex-i X-Ray System (DRAD-3000E) TFP-4336W (Wireless FPD) Software version: v5.00ER005 Product Usage: The RADREX-I is…

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

Canon Medical System, USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 17, 2019

Giraffe Infant Radiant Warmer Infant radiant warmers provide infrared heat in a controlled manner to neonates who are…

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

GE Healthcare, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 17, 2019

HAMILTON-G5, with software versions less than or equal to 2.60 The HAMILTON-G5/S1 ventilators are designed for…

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

Hamilton Medical AG

FDA (openFDA device enforcement)

Food

Reported Jul 17, 2019

Great Value Blackberries NET WT 16 OZ (1 LB) 454g bags DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716 KEEP FROZEN…

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

Riverside Foods LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 10, 2019

Powerheart¿ G5 Automatic AED

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

Cardiac Science Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jul 10, 2019

CLEO Patient Monitor /Tranquility VS Patient Monitor

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

Infinium Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 10, 2019

Vereos PET/CT, Model No. 882446 Product Usage: Positron Emission Tomography (PET) and X-ray Computed Tomography (CT)…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 10, 2019

DVR Crosslock ePAK Screw Driver, Model Number 212000002 Product Usage: These DVR Express Disposable Instruments are…

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

Zimmer Biomet, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2019

LEEP Precision Integrated System 120V, Model LP-10-120 Product Usage: The LEEP PRECISION INTEGRATED SYSTEM l 20V…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2019

Aquarius D13S319 Plus Deletion Probe, Model LPH068-A Product Usage: The D13S319 probe, labelled in red, covers a 156kb…

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

Cytocell Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2019

CIVCO Solstice(TM) SRS Immobilization System, Part Numbers: a) CHS03, b) CHS04 - Product Usage: The Tilting Head…

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

Med Tec Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 26, 2019

Maglio Companies Jalapeno Peppers sold in the following sized packages: 10 lb. Qdoba Pepper; 1-1/9 BU Pepper, Jalapeno…

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

The Fresh Group, Ltd.

FDA (openFDA food enforcement)

Food

Reported Jun 19, 2019

Cool Haus Awesome Dessert - Dairy Free Horchata Frozen Dessert Sandwich. Horchata Rice Milk & Cinnamon frozen dessert…

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

Coolhaus

FDA (openFDA food enforcement)

Medical devices

Reported Jun 19, 2019

IntraClude Intra-Aortic Occlusion Device, REF: ICF100, 10.5 Fr (3.5 mm) X 39.4" (100 cm), Rx Only, Sterile EO The…

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Food

Reported Jun 19, 2019

7-Eleven The Italian Job refrigerated sandwich, clear plastic overwrap net wt. 9.7 oz.

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

Hearthside Food Solutions

FDA (openFDA food enforcement)

Medical devices

Reported Jun 19, 2019

xTAG Gastrointestinal Pathogen Panel intended for the simultaneous qualitative detection and identification of multiple…

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

Luminex Molecular Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Jun 19, 2019

Terumo Advanced Perfusion System 1 Electronic Patient Gas System (EPGS), Electronic Gas Blender, Catalog #: 801188, UDI…

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

Terumo Cardiovascular Systems Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

MRSASelect, IVD, REF 63747, containing 20 plates per package. The MRSASelect is indicated for use in conjunction with…

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

Bio-Rad Laboratories, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

Leica Cryostats, used to produce frozen sample sections for biological, medical and industrial applications, including…

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

OMNIBotics iBlock Cutting Guide, 4146-1000 - Product Usage: The OMNIBotics iBlock Cutting Guide is a stainless-steel…

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

OMNIlife science Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV16F

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

OriGen Biomedical, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

Stryker Neurovascular, AXS Infinity LS Plus Long Sheath, Rx Only, Sterile EO, USA Customer Service 855-91 NEURO…

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

Stryker Neurovascular

FDA (openFDA device 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.