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.
Reported Jul 15, 2015
New Punjab Burfi is an Indian snack cut into 1lb or 0.5 lb. squares. Product is packaged in clear plastic container…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.New Punjab Sweets Inc.
6 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 8, 2015
Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro diagnostic.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Medtronic DLP Femoral Arterial Cannula, models 57414, 57417, and 57421, and DLP Femoral Cannula Replacement Kit, Models…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Infinite F500, in vitro diagnostic. Product Usage: The Tecan Infinite F500 is a multifunctional microplate reader with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tecan US, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Treatment Planning and Delivery System Software version 3.6. ViewRay. Indicated for stereotactic radiosurgery and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Viewray Incorporated
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Natural Knee II Revision Femoral Stem, 125mm, item 6215-12-185. packaged in configuration 803/791. Knee Prosthesis…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2015
LapSac Surgical Tissue Pouch. The current intended use for the LapSac Surgical Tissue Pouch is for isolating tissue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2015
Merit Medical Prelude Pro Sheath Introducter, 6F (2.0mm) 11cm, REF PRO-6F-11-038, Sterile EO The Merit Prelude Sheath…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2015
Chocolate covered wafers (Bocadin) in plastic packaging sold under the Mi Costenita brand and packaged and distributed…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Yoli, Inc. dba Mi Costenita
FDA (openFDA food enforcement)
Reported Jun 24, 2015
MILEX OMNIFLEX DIAPHRAGM SIZE 80 Model: MXWF80
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2015
ELI 380 Electrocardiograph. The ELI 380 is intended to be a high-performance, multichannel resting electrocardiograph.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mortara Instrument, Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2015
CADD¿- Solis Ambulatory Infusion Pump, Model 2111 & 2112, Version 1.0, Version 2.0 and Version 3.0 & Model 2120,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
FDA (openFDA device enforcement)
Reported Jun 17, 2015
AGFA DX-D 100 is a mobile digital radiography x-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Healthcare Corp.
FDA (openFDA device enforcement)
Reported Jun 17, 2015
BBL Port A Cul tubes, catalog number 221606. Patient sample collection tubes. BBL Port A Cul tubes, jars and vials…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2015
Roscoe Mini Neb Compressor User Manual for the NEB-ROS Product Usage: Inhaler therapy that converts liquid medicine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Compass Health Brands
FDA (openFDA device enforcement)
Reported Jun 17, 2015
Laksell GammaPlan, a computer based dose planning system specifically designed for use with Leksell Gamma Knife,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jun 17, 2015
Rugby Poly Vitamin Liquid, 50ml
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pharmatech LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 17, 2015
R3(TM) 22 MM I.D., 52 MM O.D. CONSTRAINED LINER, REF 71339152, QTY: (1), STERILE EO. Product Usage: The R3 Constrained…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2015
Low Volume Extension Set, 72' w/Clamp FLL/MLL APV=1.3ml, STERILE, AND FLUID PATH NONPYROGENIC UNLESS PACKAGE IS DAMAGED…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical Asd Inc.
FDA (openFDA device enforcement)
Reported Jun 17, 2015
M/L Taper with Kinectiv¿ Technology. prosthesis, hip, semi-constrained (metal uncemented acetabular component) Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Jun 10, 2015
Oncentra Brachy radiation therapy planning software designed to analyze and plan radiation treatments in three…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jun 10, 2015
Pasta salad sold under the brand name CHEF'S EXPRESS CALIFORNIA PASTA SALAD, UPC 2 10612 30070 6. Product is sold by…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Schnucks Markets Corporate Office
FDA (openFDA food enforcement)
Reported Jun 10, 2015
Tibial Alignment Guide; Orthopedic Stereotaxic Instrument;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer CAS
FDA (openFDA device enforcement)
Reported Jun 3, 2015
D2-40 (Lymphatic Marker); For In Vitro Diagnostic; Catalog number: PM266AA Product Usage: In Vitro Diagnostic Use.: a…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Biocare Medical, LLC
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.