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 Sep 14, 2022

CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath, REF: D138501. Used to introduce various cardiovascular catheters into…

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

Biosense Webster, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 14, 2022

Product Description/Item: ChemoLock Bag Spike, 10 units/CL-10-10; ChemoLock BAG SPIKE w/ ADDITIVE PORT, DRY…

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

ICU Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 14, 2022

Philips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea…

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

Philips Respironics, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 7, 2022

Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.

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

Oculus Optikgeraete GmbH

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 7, 2022

Woodland Ingredients X06D Arborio Rice, 25 lbs. bag UPC 00687080007374 Woodland Ingredients X16D Italian Arborio Rice,…

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

Woodland Foods LLC

FDA (openFDA food enforcement)

Food

Reported Sep 7, 2022

Priyems Sambar Spicy Lentil Soup 800 grams (1.76 lbs) UPC 8 61754 00010 0, 8 retail units per wholesale case, Frozen

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

Yem Foods LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 31, 2022

(1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (2) GE Centricity Universal Viewer 7.0, Model 5826659-0XX;…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable…

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

Medtronic Neuromodulation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

Nobel Biocare N1 TiUltra TCC NP 3.5x13mm

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

Nobel Biocare

FDA (openFDA device enforcement)

Meat & poultry

Reported Aug 24, 2022

FSIS Issues Public Health Alert for Poultry and Meat Products Containing FDA-Regulated Corn Starch That Has Been…

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

Fsis

USDA FSIS

Medical devices

Reported Aug 24, 2022

Power electronic box, Part #AS-0066, subassembly for the MyoCycle MC-2.

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

Myolyn Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 17, 2022

Clear American brand "Strawberry Punch Snow Cone" flavored sparkling water beverage with other natural flavors; 1-liter…

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

Refresco Beverages US Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 17, 2022

cobas e801 Immunoassay Analyzer

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10

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)

Medical devices

Reported Aug 10, 2022

The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit (ESU) designed to be used with the da Vinci Xi and…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool

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

Neotract Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

Merlin PCS 3650 programmer Model 3330 software

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

St. Jude Medical, Cardiac Rhythm Management Division

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 10, 2022

Vicks Children's Botanicals Liquid Daytime/Nighttime Combo Pack 4oz plastic bottles

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

The Procter & Gamble Company

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 3, 2022

REF: 4P52-20 Hemoglobin A1c for use with Architect, IVD, CE, R1 1 x 52 mL, R2 1 x 20 mL, A1cDL 2 x 35 mL

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

Abbott Laboratories

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 3, 2022

Da Vinci S/Si Large Clip Applier, Model 420230 Da Vinci S/Si Medium-Large Clip Applier, Model 420327 Da Vinci S/Si…

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

Intuitive Surgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 3, 2022

Lee Ann Chin Thai Peanut Sauce. In glass botle. Net Wt 13.5 oz (384g) UPC 61248 87100. Shake Well. Refrigerate After…

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

Leeann Chin, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 3, 2022

Sight OLO, Automated Hematology Analyzer, Catalog No. OLO-U1

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

Sight Diagnostics Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2022

ENDURO SPECIAL KEY TIB.LOCK.RING F1/10MM product code NP462R used with EnduRo Total Knee System. instrument used during…

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

Aesculap Implant Systems LLC

13 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2022

Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress, REF P7924A01; and REF P7924ARENT01, PRO+ MRS Rental Surface with…

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

Baxter Healthcare Corporation

6 more products in this recall

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.