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 48,100 notices were distributed nationwide, so they reach Wisconsin too — those are in the archive.
Reported Feb 12, 2020
Garlic Parmesan Sauce; DP# 4478 FG# 02620 8/16 fl. oz (4.73 ml) pouches; NET WT. 8.05 lbs (3.65 kg) Produced for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Golden State Foods
3 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 12, 2020
Legacy 3 Implant, Size: 4.2mmD x 13mmL, 3.5mmD Platform, REF: 864213
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing LLC
FDA (openFDA device enforcement)
Reported Feb 12, 2020
da Vinci Xi Surgical System Surgical System, IS4000, 00886874114216 - Product Usage: used with an endoscope, surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2020
Fresh Grab Ham & Swiss on Pretzel Sub Bun, 6 oz., UPC: 612510001028
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipari Foods Operating Company, LLC.
31 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 12, 2020
Giraffe Blue Spot PT LiteTM Phototherapy System, Model Numbers M1224917, M1231533, M1225025, M1224961, M1224958,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lumitex Inc.
FDA (openFDA device enforcement)
Reported Feb 12, 2020
Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob, 2264HAX, FFCM3205
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacific Medical Group Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 8, 2020
Family Traditions Meat Company Retira Productos De Palitos De Carne De Res Listos Para Consumir Debido A Un Error De…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Family Traditions Meat Company, Inc.
USDA FSIS
Reported Feb 5, 2020
Bard Conquest 40 PTA Dilation Catheter, 8mm X 20mm x 75cm (CQF7582), 8mm x 40mm x 75cm (CQF7584); Recommended Guidewire…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2020
CS5/5+ Fastpacks, 225 mL, 150¿ Res Autotransfusion Device - Product Usage: its related accessory components are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Haemonetics Corporation
21 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 5, 2020
Organic IntegriPure Cold Milled Flaxseed, 50 lb Net Wt. and 2000 lb. totes
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Healthy Food Ingredients, LLC
FDA (openFDA food enforcement)
Reported Feb 5, 2020
Jeni's Dairy Free Cold Brew with Coconut Cream Pints frozen dessert
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jeni's Splendid Ice Creams LLC
FDA (openFDA food enforcement)
Reported Feb 5, 2020
Healon GV PRO 0.85 mL, Model (U.S.): 10-2400-14, Model (O.U.S.): 10-2705-14, 10-2715-14, 10-2725-14, and 10-2755-14
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2020
Dimercaptopropanesulfonate Sodium (DMPS), Aqueous injection solution, 50mg/mL 5 mL SDV, Rx only, McGuff Compounding…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McGuff Compounding Pharmacy Services, Inc.
FDA (openFDA drug enforcement)
Reported Feb 5, 2020
AQURE basic sytem, FLEXLINK, REF 933-599, Version: 2.3.3 (17), CE IVD, Rx Only, UDI: (01)05700699335999 Intended use:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Feb 5, 2020
RayStation stand-alone software treatment planning system. Models 4.0, 4.3, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jan 29, 2020
TruDi NAV Suction, TDNS000Z, 0 Degree Tip Angle, (01)10705031245877
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acclarent, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2020
Imactis Navigation Kit, REF 10100, Content Sterile Needle Holder Ref. A10010 CE 0459, Sensor Cover Ref. PC3688 CE 0482,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Imactis
FDA (openFDA device enforcement)
Reported Jan 29, 2020
Soredex DIGORA Optime SOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL IMAGER)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Palodex Group Oy
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 24, 2020
Amity Packing Company Inc. Retira Productos De Carne Molida Cruda Debido A Una Posible Contaminación Con Materia Extraña
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amity Packing Co. Inc.
USDA FSIS
Reported Jan 22, 2020
ADVANCED ENDOSEE System CANNULA, Cooper Surgical Product Code/Model Number: ESPX5 The Advanced Endosee Cannula…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2020
QuickDraw Venous Cannula, REF: QD22, UDI: 00690103182699; and REF: QD25, UDI: 00690103182705
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Jan 22, 2020
Butler's Dark Chocolate with Irish Whisky, 3.52oz bar, UPC 8 44984 17619 7, 10 units per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gourmet International Ltd.
FDA (openFDA food enforcement)
Reported Jan 22, 2020
Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or cemented fixation within the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported Jan 22, 2020
LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
1 more product in this recall
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.