All recall categories

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.

Medical devices

Reported Mar 7, 2018

STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary, Secondary Administration Sets and Extension Sets (Catalog…

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

ConMed Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 7, 2018

Agility with Integrity R3.2

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

Elekta Limited

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 7, 2018

Seggiano Artichoke & Garlic Sauce & Spread Net Weight 200g, 7.1 oz, packaged in Glass jar, UPC Code: 812603020381

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

Seggiano USA Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 7, 2018

Zimmer Segmental System, ZSS Distal Femur. Sizes as follows: a. Size B-LT (Item No. 00585001201); b. Size B-RT (Item…

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

Zimmer Biomet, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 28, 2018

Innova Self-Expanding Stent System, 200 mm. Labeled with Material Number and description as follows: Product Usage: The…

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

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 28, 2018

Protura Software which utilizes Elekta's iCOM interface: MT6XSM1.4.0, MT6XSM1.4.0-1, MT6XSM1.4.0-2, MT6SXM1.4.0-3,…

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

Med Tec Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2018

Lyophilized Chemistry Calibrator Level 1 Product Usage: Beckman Coulter Chemistry Calibrators are intended for use when…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2018

EMS products from Graham Medical, SnugFit(R) Expandable Mattress Cover, Code 72930, UPC 1 07 47036 72930 3

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

Little Rapids Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2018

Video Cystoscope models ECY-1570 and ECY-1570K

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

Pentax

FDA (openFDA device enforcement)

Meat & poultry

Reported Feb 21, 2018

Triple T Specialty Meats Inc. Recalls Chicken Salad Products Due to Possible Salmonella Contamination

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

Triple T Specialty Meats Inc.

USDA FSIS

Medical devices

Reported Feb 21, 2018

A.T.S. 4000TS Tourniquet Systems, Personalized Pressure. Intended to be used by qualified professionals to temporarily…

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

Zimmer Surgical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Feb 14, 2018

FSIS Issues Public Health Alert For Poultry Products due to Possible Salmonella Contamination

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Fsis

USDA FSIS

Medical devices

Reported Feb 14, 2018

TD60 Transmitter battery charger used with the BeneVision Central Station, Part number 115-030108-00

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

Mindray DS USA, Inc. dba Mindray North America

FDA (openFDA device enforcement)

Food

Reported Feb 14, 2018

Sea Salt Caramel Hearts, Net Wt 12 OZ (340 g), Made by Palmer Candy Company, Sioux City, Iowa. UPC 77232-17091

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

Palmer and Company

FDA (openFDA food enforcement)

Food

Reported Feb 14, 2018

SunGlow, Unsalted European Style Butter Blend Margarine (16953 SNG), Net Wt 16 oz (1 lb) 454 g. Keep Refrigerated. UPC…

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

Ventura Foods LLC

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 7, 2018

Clover Valley¿ Iced Oatmeal Cookies NET WT 12 OZ (340 g) CONTAINS: WHEAT, SOY. DISTRIBUTED BY DOLGENCORP, LLC 100…

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

Dollar General Corporation, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 7, 2018

Elements Obturation Unit (EOU) used with respective Buchanan Heat Pluggers Device is an endodontic root canal plugger.…

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

Ormco/Sybronendo

FDA (openFDA device enforcement)

Medical devices

Reported Jan 24, 2018

ACCOLADE SR Pacemaker

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

Boston Scientific Corporation

23 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 24, 2018

Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) and NET WT. 3-1/2 OZ (98 g) 25 Count

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

Gel Spice Co., Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 17, 2018

Certitude Delivery System and any associated Multipacks Models - 9600CT20A, 9600CT23A, 9600CT26A, 9600CT29A Product…

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 17, 2018

UNIVERSAL FLEX2 BREATHING CIRCUIT, Item Numbers: D460-6133Z, D390-6121Z, D390-6121Z, D495-61Z, DF4116-6121Z, D466-61Z,…

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

King Systems Corp. dba Ambu, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2017

Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive investigations of heart and vascular disease when…

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

Invivo Corporation

FDA (openFDA device enforcement)

Food

Reported Dec 27, 2017

Cheddar & Sour Cream flavored Potato Chips packaged under the following brands and sizes: 1. Old Dutch Ripples, 2 oz,…

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

Old Dutch Foods, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 20, 2017

ABL800 analyzer with FLEXQ module. Device intended for in vitro testing of samples of whole blood for the parameters…

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

Radiometer America Inc.

FDA (openFDA device enforcement)

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Other states

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.