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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.

Medical devices

Reported Jan 22, 2020

Gridlock Ankle Screw Driver Bit REF 320-35-003 - Product Usage: A screwdriver facilitates implant insertion and removal.

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

Trilliant Surgical, LLC

FDA (openFDA device enforcement)

Food

Reported Jan 15, 2020

SimplySafe Sesame Seed Hulled; 49lbs bag; Lot #PBAT10025110

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

Bay State Milling Co.

FDA (openFDA food enforcement)

Food

Reported Jan 15, 2020

Simply Fresh brand MiniMeals2Go Protein Pack (8.25 OZ) ready-to-eat snack packs

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

Five Star Gourmet Foods

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 15, 2020

Cios Alpha, Model Number 10308191; mobile X-Ray system designed to provide X-ray imaging of the anatomical structures…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 15, 2020

GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT 1.4 OZ (40 G), UPC 8 53152 00308 1 , 4 OZ (113 G) UPC 8 53152…

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

TFI Holding dba Grey Ghost Bakery

FDA (openFDA food enforcement)

Medical devices

Reported Jan 8, 2020

O-arm" O2 Imaging System, Product Number/CFN: BI-700-02000

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

Medtronic Navigation, Inc.-Littleton

FDA (openFDA device enforcement)

Food

Reported Jan 8, 2020

Chef Pierre 37 Ounce Pumpkin Spice Latte Pie, in foil pie pan with dome lid, frozen, 4 pies per wholesale case, with…

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

Sara Lee Frozen Foods

FDA (openFDA food enforcement)

Medical devices

Reported Jan 8, 2020

HeartMate 3 Mobile Power Unit, REF 107754, UDI or GTIN: 00813024010883, and 107758, UDI or GTIN: 00813024010890, when…

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

Thoratec Corp.

FDA (openFDA device enforcement)

Food

Reported Jan 1, 2020

Wild Harvest Organic Unbleached All Purpose Flour, Net Wt 5 lb. (2.26 kg) in paper bags, UPC 7 11535 50915 8, 8 bags…

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

Ardent Mills LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jan 1, 2020

STA UNICALIBRATOR (ref. 00675)

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

Diagnostica Stago, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 1, 2020

Trader Joe's 8pcs Spicy California Roll, 8oz, SKU 00348966T

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

Fuji Food Products, Inc.

22 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 1, 2020

VNS Therapy, SenTiva, Model # 1000, (01)05425025750405, Rx Only for vagal nerve stimulation (VNS) therapy

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2020

PTS Panels CHOL+HDL+GLU Test Strips, Reference Number 5412, for use on CardioChek PA or CardioChek Plus analyzers

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

Polymer Technology Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2020

RayStation stand-alone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3,…

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

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2019

Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, Style 68 MP, Style…

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

Allergan PLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2019

HydroDot brand: Wave Prep 4 oz. tubes-Product 1710-03. An electroconductive cream for use with external electrodes -…

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

Bio-Signal Group Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 25, 2019

Hodgson Mill Unbleached All-Purpose White Wheat Flour 5 Lb bags 001042 Best By 10-01-2020 005517 Best By 10-02-2020

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

Cell-nique Corp. dba Living Harvest at Hudson River Foods

FDA (openFDA food enforcement)

Medical devices

Reported Dec 25, 2019

Rhondium OVC3 One Visit Crown, Model FDI 24/25L USA 12/13L A2 HT, Nonsterile, Rx. The firm name on the label is…

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

Rhondium Limited

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

Healix Knotless ADV BR 4.75 Suture Anchor

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

DePuy Mitek, Inc., a Johnson & Johnson Co.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

Monaco Radiation Treatment Planning System (RTP) System

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

Elekta Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 18, 2019

Terra Alba Calcium Sulfate Dihydrate packaged in 50 lb. bags; 25 lb. bags; 800kg (1764 lb.) bulk bags; 2000 lb. bulk…

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

Harrison Gypsum, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

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

Integra LifeSciences Corp.

41 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

VNS Therapy Program GMDN: 44077 Model # 3000 V1.5.2, RxOnly

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

Passive Biopsy Needle Kit, UDI: 00643169030121 and 00643169702943

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

Medtronic Navigation, Inc.

2 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.