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 3, 2013
Code Alert Advanced 4-Way Care Solution, CA520 System, PN 9600-1600, RF Technologies. This product is used to alert…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RF Technologies, Inc.
FDA (openFDA device enforcement)
Reported Jul 3, 2013
Quick Connect QLC1677E, QRC1699E, QPC1721E and QFC1683E. STERIS Corporation, Mentor, OH 44060 QLC1677E, QRC1699E,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Jun 26, 2013
Biomet Trauma Phoenix Retrograde Femoral Connecting Bolt Trauma Fixation Systems. Product Usage: The Phoenix Retrograde…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 26, 2013
Lightlife Farmer's Market Veggie Burgers, meat free, 12 oz/4-count bag, packaged in 5/12 oz-bag/cartons. Distributed…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Conagra Inc.
FDA (openFDA food enforcement)
Reported Jun 26, 2013
GE Healthcare, PET VCAR. PET VCAR application software is affected if installed on any of the following versions of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jun 26, 2013
Echelon, Echelon Oval and Oasis MR imaging device systems; one unit per box. The Echelon, Echelon Oval and Oasis MR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Jun 26, 2013
Tecan Freedom EVO with Touch Tools Suite Version 3.0 The intended use of the Touch Tools Suite is to run previously…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tecan US, Inc.
FDA (openFDA device enforcement)
Reported Jun 26, 2013
GlideScope Video Laryngoscope (GVL) 3, 4, 5 and GlideScope (AVL) 2, 3, 4 and 5 reusable blades Product Usage: The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Jun 26, 2013
Zimmer Patient Helper Bed Frame Adapter Assembly The bed frame adapter assembly is intended to be used by qualified…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Jun 19, 2013
Market Pantry, Sweet & Salty Mix, NET WT 3 oz (85g), UPC 0 85239 08131 0, INGREDIENTS: Peanuts (peanuts...) ...Honey…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Importing Co., Inc.
FDA (openFDA food enforcement)
Reported Jun 19, 2013
TX1 Tissue Removal System disposable handpieces. Product Usage: The TX1 Tissue Removal System is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Optisurgical Inc.
FDA (openFDA device enforcement)
Reported Jun 19, 2013
XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Atlantic Pro Nutrients, Inc. dba XYMOGEN
FDA (openFDA food enforcement)
Reported Jun 19, 2013
Blessing Brand Wild White EZ Peel Shrimp, 16/20 CT. 4 x 5 lbs cartons. The product is bagged in 5 lbs clear plastic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Blessing Seafood, Inc.
FDA (openFDA food enforcement)
Reported Jun 19, 2013
StarDental Classique(TM) Diamond Dental Bur. Used for specific applications in dental procedures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dental EZ Stardental Division
FDA (openFDA device enforcement)
Reported Jun 19, 2013
embla Embletta Gold (It functions as a Polysomnography Recorder and Ventilator Effort Recorder). The Embletta Gold is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Embla System LLC
FDA (openFDA device enforcement)
Reported Jun 12, 2013
FAST Procedure Kit. Intended for use as a Minor Surgical Procedures Tray.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Optisurgical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2013
ORIGINAL BRAND Arizona SOUTHERN STYLE UNSWEETENED Brewed Tea, Net Wt. 128 FL.OZ (1 GAL.). Product is packaged in a…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Arizona Beverages USA LLC
FDA (openFDA food enforcement)
Reported Jun 12, 2013
FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS FLEXSTENT Biliary SES product is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2013
Cottage Cheese with Chive distributed under the following labels and sizes: (a) Hood brand Cottage Cheese with Chive,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HP Hood LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 12, 2013
I-Flow ON-Q Pain Relief System, T-Block Needle/Catheter Tray, Model #TBTB1089T The intended use of each component in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.I-Flow LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2013
Comfort brand Ear-Loop Face Mask, Item #: 3100, Model Numbers: # 3100B, # 3100P, # 3100G, # 3100Y, # 3100W; Product is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maytex Corp.
FDA (openFDA device enforcement)
Reported Jun 12, 2013
BrightView SPECT gamma camera for Emission Computed Tomography, Philips Medical Systems, Cleveland, OH 44143 BrightView…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jun 5, 2013
AngioDynamics Micro Introducer Kits under the following labeling: 1) AngioDynamics 4F Standard Micro-Introducer Kit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2013
Femoral component, CR, cemented, #1, left 2103-1310 Femoral component, CR, cemented, #2, left 2103-1320 Femoral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthopedic Alliance LLC
8 more products 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.