Recalls distributed in South Dakota
These notices name South Dakota 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.
1,585 stored notices name South Dakota, reported between Jun 27, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach South Dakota too — those are in the archive.
Reported Jan 11, 2017
AMERICAN CLASSIC SUB Net Wt 6.5 oz (184g) Smoked ham, deli style bologna, hard salami with American and Swiss cheese on…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eby Brown Co.
9 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 4, 2017
Innova 2000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 4, 2017
Shimadzu X-ray TV System, Catalog No. SONIALVISION G4
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 4, 2017
SOMATOM Scope, Computed tomography x-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath¿…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Affinity Fusion" Oxygenator with Integrated Arterial Filter, Affinity Fusion cardiotomy/Venous Reservoir, Perfusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Apple Orchard Crisp Apple Hard Cider Three packages sizes: ¿ Loose case = 24 12 oz bottles ¿ 12 pack = 12 12 oz…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Samuel Adams Brewery Co.
FDA (openFDA food enforcement)
Reported Dec 21, 2016
Roasted & Salted Sunflower Kernels under the following brand names: AMISH FARMS SALEM, OHIO 44460 5.5 oz plastic bag…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ohio Hickory Harvest Brand Products Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 21, 2016
Harmony Insight Diagnostic Monitor Support System - 100 Spring Arm (EMS) The system is intended for use in surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Dec 21, 2016
Good Sense Trail Mix, Cranberries 'N More, Net Wt. 6 oz. (170g). Cranberries, Sunflower Nuts, Cashews, Pumpkin Seeds,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Waymouth Farms, Inc.
FDA (openFDA food enforcement)
Reported Dec 14, 2016
A&W Cream Soda, 20 FL OZ, Caffeine Free
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chesterman Co.
FDA (openFDA food enforcement)
Reported Dec 14, 2016
MANOS EX (CAT#TY-12-101) Product Usage: Carpal Tunnel Release: as a tool for tissue release of the transverse carpal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thayer Intellectual Property, Inc.
FDA (openFDA device enforcement)
Reported Dec 7, 2016
Monaco RTP System; Used to make treatment plans for patients with prescriptions for external beam radiation therapy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 7, 2016
Kuster's Dairy Foods Three Blend Shredded Cheese, 5 lb. packages packed in plastic bags, keep refrigerated
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kuster's Inc.
9 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 23, 2016
Version 1.2.0 of Accu-Chek Connect Diabetes Management App (iOS) released on July 11, 2016
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2016
RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Nov 16, 2016
Dorothy Lynch Homestyle 8 oz., 16 oz., and 32 oz. bottles (12/case) and 128 oz. bottles (4/case)
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Tasty Toppings Inc.
FDA (openFDA food enforcement)
Reported Nov 16, 2016
Zimmer¿ Air Dermatome II Handpiece Loaner, item number 01-8851-001-00. Device is packaged inside of a padded-foam…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
FDA (openFDA device enforcement)
Reported Nov 9, 2016
Xhibit Central Station, Model 96102. Intended use is to provide clinicians with central monitoring of adult, pediatric…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
PhoenixSpec Calibrator & Kit is used to calibrate the PhoenixSpec & Phoenix AP Instruments. The instruments are then…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 2, 2016
ex-TEM Assay for ROTEM delta Thromboelastometry System. Art. no.: 503-05 US, ex-tem. Used to monitor the coagulation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TEM Systems Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Awareness Boost Tea Dietary Supplement Passion Fruit Net Wt 7.4 oz. Distributed by & for all inquiries: Awareness…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Awareness Corporation
FDA (openFDA food enforcement)
Reported Oct 26, 2016
Nature's One, Organic PediaSmart¿ Dairy Vanilla complete nutrition beverage for kids 1 to 13 years NET WT 12.7 oz (360…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natures One Inc.
FDA (openFDA food enforcement)
Reported Oct 19, 2016
Phoenix Recon Soft Tissue Sleeve Guide, Surgical, Instrument for the sleeve and Orthopedic Manual Surgical Instruments…
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)
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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.