Recalls distributed in Minnesota
These notices name Minnesota 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.
3,845 stored notices name Minnesota, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Minnesota too — those are in the archive.
Reported May 22, 2019
Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT Estradiol assay is a Chemiluminescent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 22, 2019
Frozen ground tuna, 1 lb package, 20 packages/case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jensen Tuna Inc.
FDA (openFDA food enforcement)
Reported May 22, 2019
Pentax Medical C2 CryoBalloon Standard Focal Catheter, Model FG 1028, Sterile, RX. Product Usage: The C2 CryoBalloon…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pentax
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 22, 2019
Artis Zee (material # 10094135, 10094137, 10094141) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 15, 2019
Neuro Omega System, incorporating HaGuide software. For neurological and neurosurgical use. To monitor, record and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Alpha Omega Engineering
FDA (openFDA device enforcement)
Reported May 15, 2019
El Guapo Chile Habanero Habanero Chili Pepper 0.5oz
High riskUsing this product could cause serious injury, illness or death — stop using it now.McCormick & Company, Inc. - Flavor Manufacturing Center
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 15, 2019
Dried whole elderberry, Oregon s Wild Harvest brand, packaged in metalized plastic bag, net wt. 4 oz or 1 lb. Each case…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oregons Wild Harvest Inc.
FDA (openFDA food enforcement)
Reported May 15, 2019
Shredded and blocks of Colby & Monterey Jack cheese - Labeled and Packaged: 1) Great Value, Finely Shredded, Colby &…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Schreiber Foods Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 15, 2019
Atellica IM 1300 Analyzer, Material Number 11066001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 15, 2019
T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Biomet Headless Compression Screws and Twist-Off…
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 May 8, 2019
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), product code 35700BAX - Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported May 8, 2019
FilmArray Gastrointestinal (GI) Panel, IVD, Rx Only, Biofire Diagnostics, LLC REF: RFIT-ASY-0104, and RFIT-ASY-0116),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported May 8, 2019
Fannie May Pixies , Caramel and Pecan Clusters covered in Milk Chocolate 14 oz. Box - 12 units per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fannie May Confections Brands, Inc.
FDA (openFDA food enforcement)
Reported May 8, 2019
Cashew Brittle Bits in clear 4oz bag with a Best By date of 07/14/19 and barcode number of 00369
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hercules Candy Company
FDA (openFDA food enforcement)
Reported May 8, 2019
EZ Derm Porcine Xenograft, labeled as the following: a. EZ Derm 3x4 (8x10 cm) Non-Perforated, Part Number: 131703-03;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Molnlycke Health Care, Inc.
FDA (openFDA device enforcement)
Reported May 8, 2019
cobas e 801 immunoassay analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
FDA (openFDA device enforcement)
Reported May 1, 2019
Arthrex Burr, Oval, 12 Flute, 5.5 mm x 13 cm (AR-8550OBT) These devices are indicated for resection of soft and osseous…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported May 1, 2019
OnSight 3D Extremity System- X-Ray, Tomography Computed System Catalog Numbers: 1743566 (w/ Attached Console) 1743574…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health, Inc.
FDA (openFDA device enforcement)
Reported May 1, 2019
Edwards Lifesciences, Fogarty Dilation Atrioseptostomy Catheter, Sterile EO, Rx Only, REF: 830705F Product Usage: The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Edwards Lifesciences, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 1, 2019
Truliant Tibial Fit Tray Cemented SZ 3F / 3T, Catalog Number 02-022-45-3030 Product Usage: Knee joint…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported May 1, 2019
Fresenius Kabi CATSmart device (Continuous autotransfusion System). Labeled as the following kits: 1. AT-1 sets and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fenwal Inc.
FDA (openFDA device enforcement)
Reported May 1, 2019
Performance Series Sagittal Blade, Catalog Number 6125-127-100 Product Usage: The Stryker Heavy Duty Sagittal Blades…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported May 1, 2019
Thoratec HeartMate 3 Coring Tool, Sterile EO, Rx Only, REF 10005872, an optional accessory of Thoratec HeartMate 3 Left…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Corp.
FDA (openFDA device enforcement)
Reported Apr 24, 2019
Abbott Alinity i Processing Module LN 03R65-01 - Product Usage: The Alinity i processing module is a fully automated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
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.