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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.

1,551 stored notices name South Dakota, reported between Jun 27, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach South Dakota too — those are in the archive.

Food

Reported Mar 1, 2017

A) Palmer's Candies Chocolate Almond Bark , NET WT 9 OZ (255 g) packaged in plastic clamshell container, UPC…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Palmer and Company, dba Palmer Candy Co.

17 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 1, 2017

Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tosoh Bioscience, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 1, 2017

Keyspan High-High Speed USB to Serial Adapter Product Usage: The Reporting Software is an application which serves as…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tosoh Smd Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 22, 2017

LIFEPAK 15 Monitor, Automated External Defibrillator (AED), Manual mode monitoring and therapy functions are intended…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Physio-Control, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2017

Boston Scientific, EMBLEM S-ICD Programmer Model 3200 Programmer.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2017

Bariatric Bed - BAR600IVC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Invacare Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 1, 2017

FRONT: Stauffer's Animal Crackers Original; Net Wt. 32 OZ.; BACK: (best by date): 07SEP17; (bag lot numbers) LC120716…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

D. F. Stauffer Biscuit Co., Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 1, 2017

Hitachi Oasis MRI System - C-Spine Coil

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hitachi Medical Systems America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 25, 2017

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.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 25, 2017

PREMIER EHEC and PREMIER EHEC Bulk.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Meridian Bioscience Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2017

OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE OEC Medical Systems, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 18, 2017

IBF Peanut Butter, Net Weight 450 lbs, Hampton Farms, Severen, NC 27877.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hampton Farms Industrial Plant

FDA (openFDA food enforcement)

Medical devices

Reported Jan 18, 2017

Merge Eye Station f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2017

Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT, CR3434CT Ablation catheter cables are designed as…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Sustainability Solutions

1 more product in this recall

FDA (openFDA device enforcement)

Food

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Food

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)

Food

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)

Medical devices

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)

Food

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)

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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.