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.

Food

Reported Aug 26, 2020

Gluten-Free Organic Mesa Sunrise Cereal USA, Nature's Path brand. Shop Order # 127895. Product is Ready to eat…

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

Natures Path Foods USA, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 26, 2020

Single RIKKI Retractor, Catalog #71934609 - Product Usage: is used during surgery to hold soft tissue away from the…

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

Smith & Nephew, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 26, 2020

Earth Grown brand Mocha Fudge Non-Dairy Frozen Dessert in pint sized paperboard carton with a paperboard lid.

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

Smith Foods Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 19, 2020

HealthFirst Emergency Medical Kit, Model SM 7, P/N: 1008150; Manufactured by HF Acquisition Co. LLC, 11629 49th Place…

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

HF Acquisition Co., LLC

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 19, 2020

Garden Cut Organic Coleslaw w/ Carrots, retail unit packaged in 1lb clam-shell, 4 retail units per wholesale case,…

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

Indianapolis Fruit Company, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 19, 2020

Verigene Processor SP with assay: Luminex, VERIGENE Gram-Positive Blood Culture Nucleic Acid Test,BC-GP, IVD - Product…

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

Luminex Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 19, 2020

Tibial knee prosthesis

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

Smith & Nephew, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 19, 2020

Iron Drops (UPC 729609000098) liquid Dietary Supplement, 1 oz/30 mL amber glass bottle packaged in an individual…

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

Wellements LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 12, 2020

BD MAX SARS-CoV-2 Reagents, Cat. No. 445003 (UDI 00382904450038) and 445003-01 (UDI (01)603829044500301) - Product…

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2020

CARESCAPE ONE, Physiological Patient Monitor - Product Usage: is both a multi-parameter physiological patient monitor…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Food

Reported Aug 12, 2020

Khaotan Rice Cracker, Net Wt. 150g

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

Siam Trading Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 12, 2020

SUTUREFIX ULTRA Suture, Product number 72203855

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

Smith & Nephew, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2020

Progressa Bed, Catalog No. P7500 - Product Usage: intended to be used to treat or prevent pulmonary or other…

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

Hill-Rom, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2020

Ablation Galil Technology, IcePearl 2.0 CX 90 Cryoablation Needle, Prescription Only Galil Medicals 2.1 CX Cryoablation…

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

Boston Scientific Corporation

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2020

Thora-Para 5 Fr Non-Valved Catheter Drainage Tray

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

Carefusion 2200 Inc.

13 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2020

Software 1898072 IPC upgrade v 2.7.3.0 - Product Usage: The IPC system is indicated for the incision/cutting removal,…

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

Medtronic Xomed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2020

Nuvasive NVM5 EMG Module, REF 8020015, Rx ONLY, CE2797, Nonsterile, UDI: 00887517206633 - Product Usage: is intended…

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

NuVasive Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2020

syngo.via RT Image Suite with software versions syngo.via VB30 or VB40

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 22, 2020

BodyGuard BodySet, REF: A120-160SAS

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

CME America, LLC

36 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 22, 2020

This is an accessory to Intelect Advanced, Intelect Mobile, Intelect Neo, and V-Sonic devices. NYLATEX WRAP - Product…

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

Djo, LLC

FDA (openFDA device enforcement)

Food

Reported Jul 22, 2020

Fresh Express Iceberg Garden / Lechuga Repollo 24 oz., UPC 071279104119, iceberg lettuce, carrots & red cabbage

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

Fresh Express Incorporated

91 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 22, 2020

***KIND HEALTHY GRAINS***Oats & Honey Granola with Toasted Coconut***INGREDIENTS: Oats, tapioca syrup, brown rice, cane…

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

Kind LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jul 22, 2020

ACUMED CALLOS INJECT 10CC. Product Number: 65-0010-S, UDI: 813845020245 - Product Usage: Callos is indicated to fill…

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

Skeletal Kinetics, LLC

44 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 15, 2020

DABRA Laser (RA-308 Excimer Laser). The DABRA Laser and DABRA Catheter is an excimer laser ultraviolet light source and…

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

Ra Medical Systems, Inc.

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.