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 48,124 notices were distributed nationwide, so they reach Wisconsin too — those are in the archive.

Food

Reported Sep 26, 2012

Roundy's Rich Fields Butter Cookies. Product is labeled in part: Side of tin: "***RICH FIELDS*** Butter Cookies***NET…

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

Atico International USA, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 26, 2012

JUGGERKNOT IN¿GUIDE PUNCH, 2.9MM. The JuggerKnot 2.9mm In-Guide Punch is intended to be used to prepare a 2.9mm hole…

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

Biomet, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 26, 2012

Whole Cantaloupe. Both unlabeled and labeled "MIDWEST BEST" PRODUCE INC. HOMEGROWN CANTALOUPE #4319 PRODUCT OF THE USA

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

Chamberlain Farms Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 26, 2012

Precise Digital Accelerator Delivery of radiation to defined target volumes

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 26, 2012

Octopus 101 Perimeter; PeriTrend Software Analysis A perimeter is a device intended to determine the extent of the…

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

Haag-Streit USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 26, 2012

The 2.7mm Drilling Guide is a reusable instrument used in conjunction with a drill to prepare oriented holes in bone…

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

Integra Life Sci.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 26, 2012

Kimberly-Clark MIC Safety PEG Kit - Pull Type The Kimberly-Clark MIC PEG Kits - Pull type are Percutaneous Endoscopic…

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

Kimberly-Clark Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 19, 2012

Finest Traditions Smokey Baked Beans, 8 lbs.,10 733147 10456 6, 16 oz., 7 33147 00161 5, 8 lbs., 10 733147 10231 9;

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

Garden-Fresh Foods, Inc.

93 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 19, 2012

Sterile Empty Vial and Injector (30mL PCA vial), Rx only, One/List No. 6021-03, Hospira, Inc., Lake Forest, IL 60045.…

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

Hospira, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 19, 2012

Crown Program BK Fresh Apple Slices, 2 oz On or before August 13; no upc code

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

Missa Bay, LLC

28 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 19, 2012

Omnilife Science Apex Knee System Modular Tibia Augment, Size 1 x 4mm Ref: KC-54010. The Apex Knee System is intended…

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

Omni Life Science

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 12, 2012

BD GeneOhm MRSA ACP Assay Catalog #441637, box 48 tests labeled in part***GeneOhm Sciences Canada, Inc., 2555 boul, du…

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

Becton Dickinson & Co.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 12, 2012

Siemens Mobilett Mira. Mobile X-Ray System.

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 12, 2012

VersaTREK Windows Software, Version 5.4.3 is a component of the VersaTrek System. The Software CD will be individually…

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

Trek Diagnostic Systems

FDA (openFDA device enforcement)

Medical devices

Reported Sep 5, 2012

Siemens Stratus(R) CS Acute Care(TM) D-dimer Calibrator (DDM CalPak) lots 502058002 and 501318002 The Stratus(R) CS…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 5, 2012

syngo Imaging XS. Radiological image processing system.

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 Sep 5, 2012

QKC1692E The QKC1692E Quick Connect device connects endoscopes to the sterilization tray for C1220E liquid chemical…

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

Steris Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2012

Hitachi Echelon MRI System/Oasis MRI, Software. These are software controlled MRI devices. Product Usage: The Echelon…

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

Hitachi Medical Systems America Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 29, 2012

Menno Beachy, Cresco, IA Certified Organic Grape Tomato packaged in 1-pint square-shaped clear plastic clamshell…

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

Menno Beachy

FDA (openFDA food enforcement)

Medical devices

Reported Aug 29, 2012

syngo Dynamics Version 9.5

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

Siemens Medical Solutions, USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2012

Powered Mobility Offers Versatility (M¿V)TM Chair The Powered MOV Chair models EMS, EMS24, HHC, and INO Powered MOV…

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

Stryker Medical Division

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2012

Serial interface module RS-232 Product Usage: The System 1 provides perfusion case data transfer through the use of the…

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

Terumo Cardiovascular Systems Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 22, 2012

DePuy Custom Implant Devices Packaging: Packaging was not standardized on customs, it was dependant on the geometry of…

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

DePuy Orthopaedics, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 22, 2012

FunFresh Foods World Berry Organic Cacao Nibs 6 oz, packaged in blue, brown, red, white, black and green packaging with…

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

FunFresh Foods Inc.

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.