All recall categories

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.

Medical devices

Reported Feb 12, 2025

Temporary Titanium Abutments

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

DDS Lab

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

PROLENE Polypropylene Suture, REF: EH7585H, 8706H, 8833H, 8963H, 8935H PROLENE Suture is indicated for use in general…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ethicon, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

Ivenix Infusion System (IIS), LVP Software LVP-SW-0005. Indicated for use in a hospital and in outpatient care…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Fresenius Kabi USA, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

The Rapid fFN Specimen Collection Tube (PN: 71550-001) is a component of the Rapid fFN Specimen Collection kit (PN:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hologic, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

SenTiva, REF: 1000; SenTiva Duo, REF: 1000-D; Generators Part of the VNS Therapy System. Used for Vagus Nerve…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

LivaNova USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

UNiD" Adaptive Spine Intelligence UNiD Spine Analyzer Product Number SW3002 UDI-DI code 03613720286929 Two cloud-based…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medicrea International

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

NeiMed NasoGel for DRY NOSES UDI-DI/UPC code: 00705928045309 SKU GSP30-2R-48-ENU-USL GSP30-0R-96-ENU-USL GSP30-ARA-INTL…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Neilmed Pharmaceuticals Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

LIFEPAK 35 ECG cable REF 11111-000041

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Physio-Control, Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Feb 12, 2025

FSIS Issues Public Health Alert for Frozen Ready-To-Eat Meat and Poultry Pasties Due to Misbranding and Undeclared…

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

The Pasty Oven, Inc.

USDA FSIS

Food

Reported Feb 5, 2025

WESTCO 3065 GOLDEN BAVARIAN CREME FILLING ARTIFICIALLY FLAVORED Ingredients: Water, Sugar, Modified Food Starch,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BakeMark USA LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2025

BD Pyxis MedStation ES AUX Tower REF 343 BD Pyxis " MedStation 4000 AUX Tower REF 314 The BD Pyxis" MedStation ES and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 5, 2025

Corfu Tzatziki sauce packaged in half gallon plastic tubs, 4 tubs per case. Mediterranean Tzatziki sauce packaged in…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Corfu Tasty Gyros

FDA (openFDA food enforcement)

Food

Reported Feb 5, 2025

Alpha Test 120 count Black labeled plastic bottle, 12 bottles per case of 120 count capsules each per bottle, Store in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Iovate Health Sciences USA Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2025

Brand Name: SenTiva" Product Name: VNS Therapy" SenTiva", Model 1000 Model/Catalog Number: 1000 Software Version: NA…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

LivaNova USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2025

Medtronic PIN, 100mm STERILE PERCUTANEOUS REF: 9733235 Medtronic PIN, 150MM, STERILE PERCUTANEOUS REF: 97733236 The…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2025

BD PCR Cartridges used with MAX System. Model Number: 437519

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2025

CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810 Implantable device that provides…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Integra LifeSciences Corp.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2025

Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number: 88231 Software Version: N/A Product…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

O&m Halyard, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 29, 2025

River Valley Ranch & Kitchens Spinach Artichoke Dip Mix. net wt. 16 oz. (453g). UPC 6 92016-40021 1. Keep Refrigerated…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

River Valley Ranch Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 22, 2025

McKesson Cardiology Hemo software

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

A L I Technologies Ltd.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Model/Catalog Number: 8065977763 Product Description:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alcon Research LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

8MM, MONOPOLAR CURVED SCISSORS, IS4000 REF 470179

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intuitive Surgical, Inc.

38 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Neo-Tee T-Piece Resuscitator, for pediatric emergency respiratory support, Part: 1050805, 1050808, 1050809, 1050810,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Mercury Enterprises, Inc. dba Mercury Medical

FDA (openFDA device enforcement)

Food

Reported Jan 22, 2025

Cucumbers, Wholesale Produce Supply, 752 Kasota Circle, Minneapolis, MN 554145. Product of Mexico. Cucumbers sold in…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Wholesale Produce Supply LLC dba

FDA (openFDA food 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.