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 Jun 8, 2016
Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite Valve Product Usage: Used for aspiration of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Hip Preservation System Signature Series PreBent Burs under the following labels: 1) PreBent Spherical Bur, 5.5mm x…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Monaco RTP System Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Angel Wings Complete Daily Multi with 146 nutrients including Anti-aging and Superfruit Antioxidants and 75 Plant…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Liquid Assets Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 8, 2016
Replacement HEPA filter for Natus Sterile-Drier Model 43 and Model 44. Filter Catalogue Part Number: 54343, 54344, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Brilliance 64 Computed Tomography X-ray Systems Product Usage: Intended to produce cross-sectional images of the body…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Pronutri Re-VITA-lize Tropical Orange Dietary Supplement 32 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pronutri, LLC
FDA (openFDA food enforcement)
Reported Jun 8, 2016
Dimension Vista 500 Intelligent Lab System running on software versions V.3.6.1 SP1 or V.3.6.2, Device listing #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Reprocessed Microline Scissor Tips intended to be used with a reusable hand piece and designed for minimally invasive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sterilmed, Inc.
FDA (openFDA device enforcement)
Reported Jun 4, 2016
Solomon Snacks And Bakery Retira Del Mercado Productos De Pastel De Carne Producidos Sin El Beneficio De Una Inspeccion…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
Reported Jun 1, 2016
PerFuse Decompression Instrument PN: 800-0541, Lot:100650. Designed to access the femoral head for decompression.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
14 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2016
GE Healthcare, Discovery IGS 730. Indicated for use in generating fluoroscopic and rotational images of human anatomy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2016
Novocastra Liquid Mouse Monoclonal Antibody Calretinin, NCL-L-CALRET-566. Intended for the qualitative identification…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Jun 1, 2016
Mighty Leaf Tea Company Organic Ginger Peach Iced Tea; 100/1 oz. per case Item number 60001. UPC: 00656252600019
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mighty Leaf Tea
FDA (openFDA food enforcement)
Reported Jun 1, 2016
Bobo's Oat Bars, Gluten Free, Lemon Poppyseed, Net Weight 3 oz (85g), packaged in clear plastic, 12 bars per sleeve,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Simply Delicious Inc.
FDA (openFDA food enforcement)
Reported Jun 1, 2016
archer farms Greek-Inspired Spinach & Feta Cheese ARTISAN PIZZA, NET WT 14.9 OZ (425g). UPC Code: 0-85239-30714-4.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sinco
FDA (openFDA food enforcement)
Reported Jun 1, 2016
3.2 mm Three-fluted drill bit, sterile, Catalog ID # 03.010.060S Product Usage: Usage: The 3.2 mm Three-fluted Drill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 25, 2016
Lumenis M22 System Model Number: GA-0005400 (M22 IPL + YAG Module) with Acne Filter (KT-1014971).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lumenis Ltd.
FDA (openFDA device enforcement)
Reported May 25, 2016
Colby Jack cheese, 8 oz. and 16 oz, Vacuumed plastic pouches
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Msu Dept Of Fd Sci Dairy Plant
FDA (openFDA food enforcement)
Reported May 25, 2016
ADVIA Chemistry Triglyceride_2, concentrated; TRIG_c; Catalog # SMN # 10697575. For in vitro diagnostic use in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported May 25, 2016
COMMERCIAL WHEAT GERM 274000, 50.00 lbs. (22.68 kg); UPC Code: 0-26938-46535-3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Unfi
FDA (openFDA food enforcement)
Reported May 20, 2016
Papa John's Salads and Produce Recalls Ready-To-Eat Salad with Chicken Products Due To Possible Listeria…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Taylor Farms Southwest Inc.
USDA FSIS
Reported May 18, 2016
Direct Drive Clip Applier CA090, indicated for ligation of tubular structures or vessels in laparoscopic and general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Resources Corp.
FDA (openFDA device enforcement)
Reported May 18, 2016
Bertagni fresh Sweet Butternut Squash Ravioli, packaged in a paper tray inside a plastic bag and wrapped around with…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bertagni 1882
1 more product in this recall
FDA (openFDA food 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.