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 Jan 10, 2024
Racine Danish Kringles Raspberry Kringle, 14 oz. UPC 0 45251-00312 7. RDK Corp, Racine, WI 53404.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RDK Corp. dba Racine Danish Kringles
FDA (openFDA food enforcement)
Reported Jan 5, 2024
FSIS Issues Public Health Alert For Frozen Mushroom Risotto Products Due To Misbranding And Undeclared Allergen
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Fsis
USDA FSIS
Reported Jan 3, 2024
Alinity ci-series System Control Module, REF: 03R70-01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Jan 3, 2024
RibLoc U Plus 90 Instrument PRIMARY GUIDE ASSY, LOW PROFILE REF RBL2320 The RBL2320, Low Profile Primary Guide is an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
FDA (openFDA device enforcement)
Reported Dec 27, 2023
Abbott CELL-DYN Ruby, Model CD-Ruby, List number 08H67-01, and Abbott CELL-DYN Sapphire, Model CD Sapphire, list number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Dec 27, 2023
Ivenix Infusion System (IIS), Large Volume Pump LVP-0004
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresenius Kabi USA, LLC
FDA (openFDA device enforcement)
Reported Dec 27, 2023
Injection Needle, REF: 25207
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 27, 2023
Manischewitz Magic Max's Dark Chocolate Coins, NET WT. 0.53 OZ (15g), UPC: 072700200387 Display Box UPC: 072700200356,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kenover Marketing Corp.
FDA (openFDA food enforcement)
Reported Dec 27, 2023
Kwik Trip Cantaloupe, Item 930541. Net Wt 6 oz (170g). UPC 0 39779-00213 7. Produced & Distributed by Kwik Trip Inc.,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kwik Trip, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 27, 2023
0.9% Sodium Chloride: Brand Name: Product Name/Product Code: MAC MEDICAL: 10ML FILL SYRINGE/9210; NURSE ASSIST: 3ML IV…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nurse Assist, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 27, 2023
ACMI Roller Bar Electrodes bearing incorrect pouch label of ACMI USA Elite System and USA Series Right Angle Cutting…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Dec 27, 2023
AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported Dec 27, 2023
HMC Farms Peaches 2lb Gusset Bag
High riskUsing this product could cause serious injury, illness or death — stop using it now.The HMC Group Marketing Inc.
10 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 27, 2023
Bulk Frozen Cases: The 9" Vegan Pumpkin Pie bulk case has UPC 22518 84081 and the label is read in parts: 9" Vegan…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Willamette Valley Pie Company, LLC
FDA (openFDA food enforcement)
Reported Dec 20, 2023
Navik 3D v2, REF NAVIK3D, 3D Mapping System
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.APN Health LLC
FDA (openFDA device enforcement)
Reported Dec 20, 2023
Cut cantaloupe identified with the following Item ID and Description. 1. 11628 Cantaloupe Diced 3/4" 5lb. 2. 13075…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cut Fruit Express, Inc.
6 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 20, 2023
Sienna Bakery Chocolate Decadent Brownies (Tray)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dianne's Fine Desserts
FDA (openFDA food enforcement)
Reported Dec 20, 2023
Deli Express, Deli Club 4.4oz wedge sandwich, 10 retail units per wholesale case, UPC 41433-00157
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.E.A. Sween Co.
FDA (openFDA food enforcement)
Reported Dec 20, 2023
Acorn Raspberry Creme Filled Cookie found in gift basket: #067 Believe Cookie, Cake and Brownie Collection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Houdini Inc.
8 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 20, 2023
CereLink ICP Extension Cable (Extension Cable), Model No. 826845 Used with Codman CereLink Intracranial Pressure (ICP)…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Dec 20, 2023
Malichita brand Whole Cantaloupe 9 count and 12 count
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pacific Trellis Fruit, LLC
FDA (openFDA food enforcement)
Reported Dec 20, 2023
Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 781350. Philips Magnetic Resonance (MR)…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips North America LLC
FDA (openFDA device enforcement)
Reported Dec 13, 2023
Monarch Platform REF MON-000005-01, 100-240V- 50/60Hz 1440w
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Auris Health Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 13, 2023
BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, used with Maine Molecular Quality Controls,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device 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.