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.
Reported Jul 11, 2018
ECOLAB MICROTEK Rolled Probe Cover, 2.0 cm x 20 cm (.8 in x 8 in), Ref PC0905, packaged 1 probe cover/pouch, 25…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ecolab Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 11, 2018
microTargeting" Drive System, Product Number MT-DS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FHC, Inc.
14 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 11, 2018
St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor, Sterile EO, Model #: DM3500 The Confirm Rx ICM is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St Jude Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 11, 2018
Cannulated Driver Handle, Catalog #: 210-00-003, Rx Only, Non Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Al Reef dried apricot sour, 12 oz., packed in plastic, 24 packages per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Golden Star Wholesale Inc.
FDA (openFDA food enforcement)
Reported Jul 4, 2018
Single Chamber Temporary External Pacemaker, Model 53401
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
FDA (openFDA device enforcement)
Reported Jul 4, 2018
RayStation Radiation Therapy Treatment Planning System; 6.0, 6.1, 6.2, 7.0 Product Usage: Usage: RayStation is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Vanguard Complete Knee System; E1 Vanguard PS Tibial Bearing; Model Numbers EP-183664, EP-183642 Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2018
CritiCore Automated Urine Output and Temperature Monitor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2018
VNS Therapy Programmer, Model 3000, v1.0 System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cyberonics, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2018
CARESCAPE R860 ventilators with software version 10SP05 Product Usage: The CARESCAPE R860 ventilator is designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Datex-Ohmeda, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2018
Fabius GS Premium Anesthesia Machine; Cat. no. 8607000 Product Usage: Inhalation anesthesia machines for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 27, 2018
Kellogg's Honey Smacks, 15.3 oz. and 23 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kellogg Company
FDA (openFDA food enforcement)
Reported Jun 27, 2018
P28 JAWS Nitinol Staple System kits are designed for use in an osteotomy, arthrodesis and fragment fixation of bones…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paragon 28, Inc.
FDA (openFDA device enforcement)
Reported Jun 20, 2018
lmmunalysis EDDP Urine Control Set 1 The EDDP Urine Controls (High 125 ng/ml and Low 75 ng/ml) are used as control…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Alere San Diego Inc. dba Immunalysis Corporation
FDA (openFDA device enforcement)
Reported Jun 20, 2018
XCELA PASV 5F SL 55CM IR-145 Nitinol Wire KIT PG, Catalog Number 25-124
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics Inc. (Navilyst Medical Inc.)
37 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2018
Milk Chocolate Covered Fudge Bites, 3.75oz, PET Pouch, 12 packages per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Morley Candy Makers, Inc.
FDA (openFDA food enforcement)
Reported Jun 20, 2018
IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865350
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2018
Brilliance 64 with DEPMED HARDENING KIT 12NC: 459800191351, Model Number 728231. Computed Tomography X-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2018
Meijer DILL PICKLE FLAVORED CLASSIC CRUNCH POTATO CHIPS***UPC 719283594365***LOT CODE***
High riskUsing this product could cause serious injury, illness or death — stop using it now.Shearers Foods, LLC
FDA (openFDA food enforcement)
Reported Jun 20, 2018
Biomet Modular Primary Tibial Tray Implants; Modular Interlok Primary Tray (size 75 mm); Item No. 141215; UDI: (01)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 13, 2018
Draeger Jaundice Meter JM-103 The device is intended for use in hospitals, clinics or doctor s offices under a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 13, 2018
NaturaLyte¿ Liquid Acid Concentrate for Bicarbonate Dialysis, 3.43 Liters, Part Number: 08-3231-1 Product Usage: This…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Renal Therapies Group, LLC
FDA (openFDA device enforcement)
Reported Jun 13, 2018
Centricity PACS-IW with Universal Viewer Product Usage: Usage: Centricity PACS-IW with Universal Viewer is a device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
1 more product in this recall
FDA (openFDA device enforcement)
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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.