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.
3,965 stored notices name Wisconsin, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,842 notices were distributed nationwide, so they reach Wisconsin too — those are in the archive.
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)
Reported Jun 5, 2013
Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument - Aliquot Plunger Delivery System, 4", Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthovita, Inc., dba Stryker Orthobiologics.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2013
Peanut Butter Ribbon, 40 lb Pail, Item Numbers 07-012-40, 07-212-40, and 49-00100-40, Manufactured by Pecan Deluxe…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pecan Deluxe Candy Company
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 5, 2013
45 mm Screw, Item #BG7045 Product Usage: Spinal Solutions distributes a variety of spinal fixation devices in loaner…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spinal Solutions, LLC
9 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2013
***REF S-3D*** 3mm Diamond Ball. Used for cutting and shaping bone.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported May 29, 2013
Cardinal Health hCG Cassette Rapid Test, Part Number: B1077-22 (Mfg PN: 4582105026) The SP hCG Cassette Rapid Test is a…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Alere San Diego, Inc.
FDA (openFDA device enforcement)
Reported May 29, 2013
MyRay RXDC dental unit x-ray unit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cefla Dental Group
FDA (openFDA device enforcement)
Reported May 29, 2013
Krinos TAHINI ground sesame seeds, 1) Net. Wt. 1 lb (454g) in glass jars with gold lids packed 12 jars per case - UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Krinos Foods, Inc.
FDA (openFDA food enforcement)
Reported May 29, 2013
Ref: VP1600 HD Still Capture System ConMed Linvatec . Captures, stores and transfers images generated by a medical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Linvatec Corp. dba ConMed Linvatec
FDA (openFDA device enforcement)
Reported May 29, 2013
Brilliance CT 16-Slice Water, System Code: 728245; Brilliance CT 10-Slice Water, System Code: 728250; Brilliance CT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported May 29, 2013
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Modified Coated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Progressive Medical Inc.
16 more products in this recall
FDA (openFDA device enforcement)
Reported May 29, 2013
Stryker Orthopaedics Triathlon Femoral Distal Augment- Left; 1 single unit per package Howmedica Osteonics Corp. 325…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported May 22, 2013
AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control System is used to treat urinary incontinence due to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 22, 2013
Liquichek" ToRCH Plus IgM Control - Positive Liquichek ToRCH Plus IgM Control is intended for use as an unassayed…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Bio-rad Laboratories, Inc.
FDA (openFDA device enforcement)
Reported May 22, 2013
Proplege Coronary Sinus Catheter model PR9, 11 French Introducer, kitted with PR9. Product Usage: The catheter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported May 22, 2013
GE Healthcare Innova 2100 IQ, Innova 3100 IQ, Innova 4100 IQ, Innova 2121 IQ, Innova 3131 IQ , Innova 3100, Innova…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported May 22, 2013
Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Heartware Inc.
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.