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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 48,122 notices were distributed nationwide, so they reach Wisconsin too — those are in the archive.

Food

Reported Dec 19, 2018

Imperial Taste Fried Red Onion, Cu Hanh Phi; 24 x 8oz. Item #1760, UPC Code: 741861017607; 24 x 12oz. Item #1761, UPC…

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

Gemini Food Corporation Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 19, 2018

Medtronic HeartWare Ventricular Assist HVAD System Battery Charger Model 1600US - Product Usage: The HeartWare…

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

Heartware, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 19, 2018

UroLift System REF Catalog Number: UL400-4 Tray Contents: UroLift System with Handle Release Tool STERILE R CE 0050…

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

Neotract Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 19, 2018

HeartStart MRx, Rechargeable Li-Ion (lithium ion battery), REF: M3538A, which is a component of HeartStart MRx…

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 12, 2018

Optional MDRC-1119 Front Cover Attachment Kit for review display monitors. Product Usage: The product is an optional…

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

Barco N.V.

FDA (openFDA device enforcement)

Food

Reported Dec 12, 2018

Parsley Flakes in 6 oz. and 24 oz. plastic bottles and 20 lb boxes

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

Black River Industries

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 12, 2018

Captus 3000 Thyroid Uptake System, Model # 5430-0076 and 5430-0077

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

Capintec Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 12, 2018

16 count Smartfood Delight Variety Pack Sack

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

Frito-Lay, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 12, 2018

NOW Vitamin B-50 Complex with C 100 Veg Caps

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

NOW Foods

FDA (openFDA food enforcement)

Medical devices

Reported Dec 12, 2018

STEPHANIX D2RS Digital Dynamic Remote Systemhttp://cts.fda.gov/division-tracking/images/trash.png Product The D2RS…

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

Stephanix

FDA (openFDA device enforcement)

Food

Reported Dec 5, 2018

Organic Cardamom Green Whole. Product of Guatemala. Product is labeled with a paper label son onto each 25-kg…

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

New Forest LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 28, 2018

Ascom Telligence Nurse Call System

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

Ascom (US) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2018

The SQ-RX Pulse Generator a component of the Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System The…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Food

Reported Nov 28, 2018

DIDGFPGB, Food Grade Pre-Gel Corn Flour. Bulk

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

Fairview Mills Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 28, 2018

Irrisept OR, Finished Bottle Assembly 450 ml STEP 1

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

Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2018

Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 (Model: Minicon…

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

Merck Millipore Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

Arrow AGB+ Multi-Lumen CVC Kit, 7 Fr., 3 Lumen, 20cm catheter length, .025 inch dia. spring-wire guide, Product Code…

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

Arrow International Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

3.2mm Proximal Reamer/Cannulated Drill provided as part of the Fibulock Fibular Nail System Pack. FibuLock Nail…

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

Arthrex, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

-Outer Kit Box (P/N RFIT-LBL-0140) - FilmArray¿ Meningitis/Encephalitis (ME) Panel REF RFIT-ASY-0118 30 For FilmArray…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

bioM¿rieux NucliSENS easyMAG Lysis Buffer ref. 280134

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

bioMerieux, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

GE Healthcare Millennium MyoSIGHT Nuclear Cardiology Imaging System H3000ZH Acquisition System

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

GE Healthcare, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option

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

Stryker Medical Division

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 21, 2018

Chef Sensations Fire Roasted 1/2" diced onion/pepper blend Net Wt 20 lbs

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

The Wornick Company

FDA (openFDA food enforcement)

Medical devices

Reported Nov 21, 2018

Affixus Hip Fracture Nail Left Deg 9x300mm, Item Number 814609300 The Affixus Hip Fracture Nail System, comprised of…

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

Zimmer Biomet, Inc.

7 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.