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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 Jan 1, 2014

Macaroni Reg CAD, Formula MA.50, Macaroni Salad, packaged: -7-Eleven Fresh to Go Macaroni Salad, 12/7-oz carton cases.…

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

Reser's Fine Foods, Inc.

212 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 1, 2014

Ziehm Vista/Vista Plus C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging

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

Ziehm Imaging Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 25, 2013

Nature's Way, UPC 33674149263, Alive Whole Food Energizer with Iron, 60 Tabs 20009807; Nature's Way, UPC 33674149270,…

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

Schwabe North America, Inc.

12 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 25, 2013

Dimension(R) TACR Flex(R) reagent cartridge (DF107) The TACR method is an in vitro diagnostic test intended to…

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)

Medical devices

Reported Dec 18, 2013

Product is labeled in part: LIST NO. 43449; RECEPTAL CANISTER; DO NOT FILL 900 ABOVE THIS LINE; Product of China;…

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

Hospira Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2013

AMSCO¿ Evolution¿ steam sterilizer Transfer Carriage. Product Usage: Mobile, wheeled transportation unit utilized to…

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

Steris Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2013

Helion S Exam Light or H300 The device is intended to locally illuminate an examination area of the patient's body with…

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

Trumpf Medical Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 4, 2013

Mozzarella String Cheese made with 2% milk for 1/4 less fat, sold under Kraft brand or Polly-O brand and packaged with…

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

Kraft Foods Group

7 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 27, 2013

GE Healthcare Discovery NMCT 670, Discovery NM 630, Optima NMCT 640, & Brivo NM 615. The GE Discovery NMJCT 670 system…

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

GE Healthcare, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2013

The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the…

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

Hospira Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2013

Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ, CGRLS190HS, CGRLS190S, CGRLS300HS, CGRLS300S. CGRXT190HJ,…

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

Medtronic Vascular

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2013

VITROS Chemistry Products ACET Slides, 90 slides/pack; catalog number 1037274 VITROS Chemistry Products ACET Slides…

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

Ortho-Clinical Diagnostics

36 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2013

AW VolumeShare 4 (ADVANTAGE WORKSTATION 4.3.), AW VolumeShare 5 (AW VOLUMESHARE 5 WITH ANGIOVIZ OPTION), AW Server.…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2013

Plum A+ Hyperbaric Infusion Pump; List Number 11005; Labeled in part: PLUM A+ HYPERBARIC; Product Usage: The Plum A+…

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

Hospira Inc.

14 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 13, 2013

Angel Food Cake; labeled for retail sale in the following stores: Safeway, Carrs, Dominicks, Genuardis, Pak N Save,…

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

Safeway Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Nov 6, 2013

the Snack Artist BBQ Flavored Potato Chips, Net Wt. 10 oz. (283 g), UPC 21130-29106. Distributed by Safeway, Inc.…

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

Barrel O' Fun Snack Foods Co.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 6, 2013

Cordis OPTEASE Vena Cava Filter Is indicated for use in the prevention of recurrent pulmonary embolism (PE) via…

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

Cordis Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2013

PIPELINE LS ACCESS SYSTEM, 15 Dilator, 5 mm, Insulated The PIPLINE LS Dilators and Holding Clip are intended for…

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

DePuy Spine, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2013

The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by…

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

GE Healthcare It

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2013

MAQUET Getinge Group CARDIOHELP Base Unit REF 70104.7999 REF 70104.8012 Manufactured for: MAQUET Cardiopulmonary AG…

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

Maquet Medical Systems USA

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2013

pocH-100i; sysmex; Automated Hematology Analyzer; 7.3" x 13.8" x 18.1" / 30.8 lbs.; Sysmex Corporation; 1-5-1…

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

Sysmex America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 23, 2013

Getinge 46-Series Medical Washer-Disinfectors, Listing # E208196 Product Usage: The washer disinfector is used in…

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

Getinge Disinfection

FDA (openFDA device enforcement)

Medical devices

Reported Oct 9, 2013

Lactate Membrane units for E7077 Electrode Radiometer Medical ApS. The intended use is in vitro testing of samples of…

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

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2013

Invacare Power Wheelchair, one per box To provide mobility to a person restricted to a sitting position.

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

Invacare Corporation

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.