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 Nov 28, 2012
IO Fix IntraOsseous Fixation System; Extremity Medical. www.extremitymedical.com; Customer Service: 888.499.0079. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Extremity Medical LLC
FDA (openFDA device enforcement)
Reported Nov 28, 2012
KING LAD SILI CONE SINGLE USE, King Systems devices/case, ETO Sterile. Size 2 / Infant Silicone King LAD¿ Patient Size:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.King Systems Corp.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 28, 2012
The RIO (TGS 2.), Model # MAKO TGS 2.0 (Part No. 204000). The RIO is intended to assist the surgeon in providing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Screw Tulip , 6.25mm Rod Subsequent Codes: KWP, KWQ, MNH, MNI
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Inc.
30 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Dimension Vista(R) Systems Vista(R) Theophylline THEO Flex(R) Regent Cartridge (K4071) The THEO method is an in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Styker Orthobiologics Vita Plasma Separator, a component of Vitagel Surgical Hemostat. Sterile, single use device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Orthobiologics, Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2012
Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm), Reorder Number: PMILK40, Product Sterile in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Progressive Medical Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2012
Aunt Marie's Bakery Gourmet Cookie Dough, Chocolate Chunk, packaged in 3-lb. plastic tubs. Distributed by Racine Danish…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RDK Corp.
FDA (openFDA food enforcement)
Reported Nov 21, 2012
HX2 Temp Manage SYS 120V The Terumo HX2 Temperature Management System is a selfcontained, dual channel system for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
7 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 14, 2012
Cliniqa Liquid QCTM Cardiac Marker Control for i-STAT Level 1 (List Number 06F12-09; Lot Number 071039) Cliniqa Liquid…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Abbott Point Of Care Inc.
FDA (openFDA device enforcement)
Reported Nov 14, 2012
TI Standard Polyaxial Screw Assembly 6.5MM x 55MM. Part # 62065-55. Subsequent Product Codes: MNH, MNI. The Zodiac…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alphatec Spine, Inc.
FDA (openFDA device enforcement)
Reported Nov 14, 2012
Chocolate Peanut Butter Non-Dairy Frozen Dessert is sold under brand Luna & Larry's Organic Coconut Bliss. It is…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bliss Unlimited
FDA (openFDA food enforcement)
Reported Nov 14, 2012
Boule Con-Diff Hematology Control For in vitro diagnostic use as a control to monitor the performance of…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Clinical Diagnostic Solutions
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 14, 2012
Dole American Blend; Iceberg, Romaine, Red Cabbage, Carrots and Radishes. Net Wt. 12 oz. (340g) UPC 0 71430 00933 8…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dole Fresh Vegetables Inc.
FDA (openFDA food enforcement)
Reported Nov 14, 2012
Starbucks Protein Bistro Box, Net Wt 6.8 OZ (193g), Contains Cage-free egg, white Cheddar Cheese, multigrain muesli…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Flying Food Group, Inc.
FDA (openFDA food enforcement)
Reported Nov 14, 2012
Pinnacle3 VCC P/N 4598 001 41341 REV A, Philips Medical Systems (Cleveland), Inc., Fitchburg, WI. Pinnacle3 Radiation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland), Inc.
FDA (openFDA device enforcement)
Reported Nov 14, 2012
Siemens Dimension Vista(R) Homocysteine Flex(R) Reagent Cartridge This is an in vitro diagnostic test for the…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 7, 2012
HeartSine Samaritan(R) 300/300P PAD devices with serial numbers 0400000501 to 0700032917; 08A00035000 to 10A0070753;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartsine Technologies, Limited
FDA (openFDA device enforcement)
Reported Nov 7, 2012
Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm), Reorder Number: PMILK40, Product Sterile in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Progressive Medical Inc.
FDA (openFDA device enforcement)
Reported Nov 7, 2012
Ma Baensch Marinated Herring in Wine Sauce, Net Wt. 24 oz.. (680g), UPC 714449-10220 in glass jars with gold metal lids.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wild Foods, Inc.
FDA (openFDA food enforcement)
Reported Oct 31, 2012
GE Seno Advantage 1.x, Seno Advantage 2.0, Seno Advantage 2.1 Seno Advantage 1.x, Seno Advantage 2.0, Seno Advantage…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2012
Kraft Jalapeno String Cheese, Net Wt 12 Oz (340 g); a natural low-moisture part-skim mozzarella cheese with jalapeno…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kraft Foods, Inc.
FDA (openFDA food enforcement)
Reported Oct 31, 2012
Gish 3/8 x 3/8" Straight Connector with Luer fitting, Item Numbers: EC2160B, EC2160S, Lot Numbers: 1210100010,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2012
Perfusion System 8000, base 4 pump, 115V safety monitor included The Sarns Modular Perfusion System 8000 is indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
5 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.