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 Oct 13, 2021
Access hsTnI High Sensitivity Troponin I, REF B52699 Access Immunoassay System REAGENT PACK
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Oct 13, 2021
CardioQuip, Modular Cooler-Heater, Model: MCH-1000(i), CE 2797, UDI: (01)00860000846103
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CardioQuip, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 13, 2021
Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Contamac Solutions, Inc.
FDA (openFDA device enforcement)
Reported Oct 13, 2021
ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee joint replacement Part Code:152307001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Oct 13, 2021
GEL CONDUCTOR, Description/REF: 5 LITER W/DISP/4238, 24-8.5OZ BOTTLES/4248, 5 LITER/4266, distributed by DJO, LLC / DJO…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Djo, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 13, 2021
Zoll REF: 8700-0782-01 (IC-3893), ICY Intravascular Heat Exchange Catheter Kit, with central venous infusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZOLL Circulation, Inc.
27 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 6, 2021
Vysis CLL FISH Probe Kit with the following components: Vysis LSI p53 SpectrumOrange/ATM, SpectrumGreen and LSI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Molecular, Inc.
FDA (openFDA device enforcement)
Reported Oct 6, 2021
PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM Catalog Number: FC700SU
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Implant Systems LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 6, 2021
Corin TriFit TS, Size 8, Standard Tapered Stem, REF 694.0008, Sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Corin Ltd.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 6, 2021
Elekta Monaco - Product Usage: used to make treatment plans for patients with prescriptions for external beam radiation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta Inc.
FDA (openFDA device enforcement)
Reported Oct 6, 2021
uMI 550 System - Product Usage: intended to be operated by qualified healthcare professionals to assist in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shanghai United Imaging Healthcare Co., Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 29, 2021
Centricity PACS-IW with Universal Viewer - Product Usage: Is a device that displays medical images (including…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 29, 2021
CoLink Bone Graft Harvester, 8mm, Sterile, Disposable, REF G05 S1008 - Product Usage: is a general instrument intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.In2bones USA, LLC
FDA (openFDA device enforcement)
Reported Sep 29, 2021
DLP Left Heart Vent Catheters, 16 FR. Sterile, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 29, 2021
SARS-CoV-2 Process Control (Pellet) - Product Usage: intended for use as an external, non-viable control material to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 29, 2021
EPIQ Diagnostic Ultrasound Systems: Software Versions 5.0, 5.0.1 and 5.0.2 Models: EPIQ 5 - 795120 EPIQ 5C - 795205…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 29, 2021
cobas SARS-CoV-2 & Influenza A/B Test for use on the cobas Liat System, Catalog Number 09211101190
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Molecular Systems, Inc.
FDA (openFDA device enforcement)
Reported Sep 22, 2021
BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES, REF: 20019E
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion
14 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 22, 2021
Cellex qSARS-Cov-2 Antigen Rapid Test, 25 tests/box, submitted as EUA202955 "declined to issue"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cellex
FDA (openFDA device enforcement)
Reported Sep 22, 2021
Arjo Disposable Repositioning Sling, Model AHD001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge Dominican Republic SA
FDA (openFDA device enforcement)
Reported Sep 22, 2021
Marketside Chocolate Candy Cookie Cake, 24 oz. 12 x 12 black tray with clear lid.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jimmy's Cookies, LLC
FDA (openFDA food enforcement)
Reported Sep 15, 2021
Pipeline Flex Embolization Device
High riskUsing this product could cause serious injury, illness or death — stop using it now.Micro Therapeutics Inc.,
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 13, 2021
SAS Foods Enterprises Inc. Recalls Frozen, Fully Cooked Beef and Chicken Empanada Products Packaged without Benefit of…
High riskUsing this product could cause serious injury, illness or death — stop using it now.SAS Foods Enterprises Inc.
USDA FSIS
Reported Sep 8, 2021
BrightFarms Sunny Crunch; packaged in clear, plastic clamshells; 4oz and 8oz; grown at the company's Rochelle, Illinois…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bright Farms
9 more products in this recall
FDA (openFDA food 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.