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 5, 2014
Family Gourmet Long Grain Enriched White Rice in 32 oz. clear plastic bags (SKU: 1218898) and 80 oz. clear plastic bag…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Family Dollar Stores - NC Distribution Center
FDA (openFDA food enforcement)
Reported Nov 5, 2014
The GemStar Power Supply is an accessory for the GemStar Infusion Pump. It is a two piece assembled switching power…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 5, 2014
Merge Healthcare, Merge Hemo Programmable diagnostic computer. The system comprises the Patient Data Module and the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Nov 5, 2014
Covidien Puritan Bennett 980 Ventilator, Rx ONLY. Suitable for service in a hospital (institutions) and intra-hospital…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nellcor Puritan Bennett Inc. (dba Covidien LP)
FDA (openFDA device enforcement)
Reported Nov 5, 2014
ACCU-CHEK Spirit Combo insulin infusion pump sold as part of Accu-Chek Combo System Product Usage: The ACCU-CHEK Combo…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Oct 29, 2014
Box Label: 3 mm Cueva Electrode Kit, Sterile EO, Rx Only, REF. CNE1-3KDINX . Pouch labels: Each kit contains 3 pouches.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ad-Tech Medical Instrument Corporation
FDA (openFDA device enforcement)
Reported Oct 29, 2014
SWISS CHOCOLATE CHOCOLAT ALPROSE 52% CACAO PREMIUM DARK CHOCOLATE, within stand-up maroon colored gift box. NET WT 3.5…
High riskUsing this product could cause serious injury, illness or death — stop using it now.BBM Chocolate Distributors, Ltd.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 29, 2014
Frozen battered onion rings packaged in 40 oz plastic bags, 6/case under the following private labels: (1) Imperial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McCain Foods USA
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 29, 2014
Mortara Surveyor S12 and Surveyor S19 Patient Monitors. Product Usage: They are indicated for use in adult &…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mortara Instrument, Inc.
FDA (openFDA device enforcement)
Reported Oct 29, 2014
Symbia E is a multi-purpose SPECT system ideal for hospitals and outpatient centers. It is used to detect or image the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 29, 2014
DePuy Synthes Radiolucent Retractor, part number 387.580, lot number 3620715
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes, Inc.
FDA (openFDA device enforcement)
Reported Oct 22, 2014
Omni Micro-electrode/reference electrode for cobas b221 analyzer. The Roche Diagnostics Omni S Analyzer is a fully…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Oct 22, 2014
Stryker T2 Tibia System Nail Insertion Sleeve, Elastic, Sterile, a) REF 1806-1406S, SPI 08-11 and b) REF 1806-1407S,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported Oct 15, 2014
ArjoHuntleigh Contoura C1000 series beds are designed to accommodate patients weighing up to 990 lbs. (450 kg). Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arjo Hospital Equipment AB
FDA (openFDA device enforcement)
Reported Oct 15, 2014
RECLAIM Distal Reamer Extension Non Sterile REF 2975-00-500 Intended as an attachment device to the distal reamers to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 15, 2014
Hostess Frosted Bagged Donettes, 11.25 oz
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hostess Brands LLC
5 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 15, 2014
Mars Chocolate North America Milk Chocolate M & M's Net Wt. 3.40 oz packed in a brown, 3 inch x 6.5 inch cardboard box…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mars Chocolate North America
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 15, 2014
Nemschooff, Model Numbers - Serenity II:790-12, Serenity III: 791-12, Serenity III Exam: 791-12E, and Serenity IIS:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nemschoff Chairs, Inc.
FDA (openFDA device enforcement)
Reported Oct 15, 2014
MaxLock Extreme Mod-Foot Concave Reamer; Individually packaged in a 3 x 4 bag and heat sealed with label on the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthohelix Surgical Designs Inc.
FDA (openFDA device enforcement)
Reported Oct 15, 2014
Protocol 10% NBF Product Usage: 10% NBF is used to store and fixate tissue prior to grossing and histological…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Richard-Allan Scientific Company
6 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 8, 2014
GE Healthcare Precision 500D, Classical R&F System. Product Usage: The Precision 500D R&F X-ray System is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Oct 8, 2014
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumed International, Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 8, 2014
Verigene BC-GP Kit (Catalog number 20-005-018); 1) 20 Verigene BC-GP Test Cartridges; are qualitative multiplexed in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nanosphere, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 8, 2014
The Symbia T Series consists of the T16, T6, T2, and T. The Symbia T integrates state-of-the-art SPECT and high quality…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
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.