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 Dec 26, 2018
Kitchen Cravings Mixed Berry Parfait, Net Wt 8.25 oz (234g) Creamy Parfait Base, Strawberries & Blueberries with…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kwik Trip, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 26, 2018
Inspired Organic Sunflower Butter 16oz. plastic jar, 6 per case UPC #: 863669742526 refrigerate after opening
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipari Foods Operating Company, LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 26, 2018
Milk Chocolate Maltballs: NET Wt. 15 lbs. Item number 992 Case UPC 00797817-00992-9 Allergy Information: This product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Marich Confectionery Company, Inc.
FDA (openFDA food enforcement)
Reported Dec 26, 2018
Kwik Trip Granola, Bulk Granola, 09976. Net Wt 20 lbs / 9.1 kg. Manufactured by: Oakhouse Bakery, 2221 Mustang Way,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oakhouse Bakery
FDA (openFDA food enforcement)
Reported Dec 19, 2018
Imperial Taste Fried Red Onion, Cu Hanh Phi; 24 x 8oz. Item #1760, UPC Code: 741861017607; 24 x 12oz. Item #1761, UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gemini Food Corporation Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 19, 2018
Medtronic HeartWare Ventricular Assist HVAD System Battery Charger Model 1600US - Product Usage: The HeartWare…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Heartware, Inc.
FDA (openFDA device enforcement)
Reported Dec 19, 2018
UroLift System REF Catalog Number: UL400-4 Tray Contents: UroLift System with Handle Release Tool STERILE R CE 0050…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neotract Inc.
FDA (openFDA device enforcement)
Reported Dec 19, 2018
HeartStart MRx, Rechargeable Li-Ion (lithium ion battery), REF: M3538A, which is a component of HeartStart MRx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Dec 12, 2018
Optional MDRC-1119 Front Cover Attachment Kit for review display monitors. Product Usage: The product is an optional…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Barco N.V.
FDA (openFDA device enforcement)
Reported Dec 12, 2018
Parsley Flakes in 6 oz. and 24 oz. plastic bottles and 20 lb boxes
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Black River Industries
2 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 12, 2018
Captus 3000 Thyroid Uptake System, Model # 5430-0076 and 5430-0077
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Capintec Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 12, 2018
16 count Smartfood Delight Variety Pack Sack
High riskUsing this product could cause serious injury, illness or death — stop using it now.Frito-Lay, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 12, 2018
NOW Vitamin B-50 Complex with C 100 Veg Caps
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.NOW Foods
FDA (openFDA food enforcement)
Reported Dec 12, 2018
STEPHANIX D2RS Digital Dynamic Remote Systemhttp://cts.fda.gov/division-tracking/images/trash.png Product The D2RS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stephanix
FDA (openFDA device enforcement)
Reported Dec 5, 2018
Organic Cardamom Green Whole. Product of Guatemala. Product is labeled with a paper label son onto each 25-kg…
High riskUsing this product could cause serious injury, illness or death — stop using it now.New Forest LLC
FDA (openFDA food enforcement)
Reported Nov 28, 2018
Ascom Telligence Nurse Call System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ascom (US) Inc.
FDA (openFDA device enforcement)
Reported Nov 28, 2018
The SQ-RX Pulse Generator a component of the Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Nov 28, 2018
DIDGFPGB, Food Grade Pre-Gel Corn Flour. Bulk
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fairview Mills Inc.
FDA (openFDA food enforcement)
Reported Nov 28, 2018
Irrisept OR, Finished Bottle Assembly 450 ml STEP 1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
FDA (openFDA device enforcement)
Reported Nov 28, 2018
Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 (Model: Minicon…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merck Millipore Ltd.
FDA (openFDA device enforcement)
Reported Nov 21, 2018
Arrow AGB+ Multi-Lumen CVC Kit, 7 Fr., 3 Lumen, 20cm catheter length, .025 inch dia. spring-wire guide, Product Code…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2018
3.2mm Proximal Reamer/Cannulated Drill provided as part of the Fibulock Fibular Nail System Pack. FibuLock Nail…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2018
-Outer Kit Box (P/N RFIT-LBL-0140) - FilmArray¿ Meningitis/Encephalitis (ME) Panel REF RFIT-ASY-0118 30 For FilmArray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Nov 21, 2018
bioM¿rieux NucliSENS easyMAG Lysis Buffer ref. 280134
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Wisconsin recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.