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 Jul 29, 2026

Flexible Hystero-Fiberscope Kits REF: 11264BBU1, 11264BBUK1, that contain expired Single Use Endoscopic Seal: GYN, REF:…

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2026

MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2026

Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT

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

Penumbra, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 22, 2026

Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ. (411 g) Microwave: Place soup in a microwave-safe bowl.…

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

Amy's Kitchen Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 22, 2026

da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13, 430013-15

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 22, 2026

functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY NET WT. 12 OZ…

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

Nutricia North America

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 22, 2026

Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number: M101, Unilateral orthopedic/trauma external fixation device

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

Orthofix U.S. LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 15, 2026

Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS…

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

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jul 15, 2026

Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote Afterloading Applicator Product…

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

Elekta, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2026

OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG1260T SAFE-T-CENTESIS TRAY 6FR X 16CM UDI-DI…

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

Bard Access Systems, Inc.

13 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2026

Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 Product Codes that include the…

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

Covidien LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2026

Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1…

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

Hamilton Medical AG

1 more product in this recall

FDA (openFDA device enforcement)

Consumer products

Reported Jul 8, 2026Updated Sep 16, 2026

Oribe Serene Scalp Densifying Shampoo, packaged in 8.5 fl. oz. (250 mL) bottles with UPC 840035231242 and 33.8 fl. oz.…

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

KAO USA Inc.

FDA (weekly enforcement report)

Food

Reported Jul 8, 2026

MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein Vegan Nuggets, Net Wt. 10.5 oz. (298g), packaged in a…

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

Mars Snacking

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 8, 2026

Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips…

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

Teleflex LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2026

GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers (by Region) United States (includes…

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

W L Gore & Associates, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 8, 2026

Plastic 1-gallon clear pail blue label which reads in part as "BLUE RIBBON CLASSICS FRENCH VANILLA, MFD. BY WELLS…

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

Wells Enterprises, Inc.

FDA (openFDA food enforcement)

Drugs

Reported Jul 1, 2026Updated Sep 16, 2026

Determine HIV 1/2 Ag/Ab Combo 25T, Model/Catalog No. 7D2648

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

Abbott Diagnostics Scarborough, Inc.

FDA (weekly enforcement report)

Medical devices

Reported Jul 1, 2026

Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe Screw; 3070-27009 2.7mm x 9mm NL…

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

Acumed LLC

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2026

6/11oz Sunflower Seeds Salted

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

George J Howe Company, Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2026

Da Vinci ASSY, PSS, SP1098, Part Number: 380601

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 1, 2026

INZONE DETACHMENT SYSTEM, REF: M00345100950

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

Stryker Neurovascular

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2026

1.5oz Zapp's Bayou Blackened Ranch Kettle Chips, Plastic Bag.

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

Utz Quality Foods, LLC

5 more products in this recall

FDA (openFDA food enforcement)

Meat & poultry

Reported Jun 25, 2026

FSIS Issues Public Health Alert for Ready-To-Eat Chicken Caesar Wrap Products That May Be Contaminated With Listeria

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

Taher, Inc.

USDA FSIS

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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.