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.

1,585 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.

Medical devices

Reported Mar 16, 2016

Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J; Indicated for use in the prevention of…

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

Bard Peripheral Vascular Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 16, 2016

Spacelabs Healthcare Xhibit Central Station, Model 96102 is used to provide clinicians with central monitoring of…

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

Spacelabs Healthcare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 16, 2016

ROTROL P Control for ROTEM delta Thromboelastometry System, For In Vitro Diagnostic Use Only. Quality control material…

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

TEM Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 16, 2016

M/L Taper Hip Prosthesis (Item: 00-7711-012-20, Lot: 62937093

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

Zimmer Biomet, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 9, 2016

Braga Organic Farms Organic Pistachio Kernels, Raw; Certified Organic, USDA Organic. Packed in 8 oz. 1 lb. 2. lb and 5…

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

Braga Organic Farms, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 9, 2016

Heartland Flax 14 Mesh Brown RCM Flax Certified Organic, Net WT 50 lbs. Product packaged in 50 lb Food Grade Plastic…

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

Heartland Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 9, 2016

BrightView are gamma cameras; Designed for single or dual detector nuclear imaging.

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

Philips Medical Systems (Cleveland) Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2016

Endobon-Xenograft Granules, Zimmer Biomet, Synthetic Bone Grafting Material, used in dental and/or surgical procedures.…

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

Biomet France SARL

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2016

Arctic Sun 5000 and Arctic Sun 2000; Intended for monitoring and controlling patient temperatures.

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 10, 2016

API ZYM Bx2 (Ref 70493) Product Usage: ZYM B reagent is an additional test used for revealing the results of some…

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

BioMerieux SA

FDA (openFDA device enforcement)

Medical devices

Reported Jan 27, 2016

The e.cam Dual Signature Gamma Camera system. Used to detect or image the distribution of radionuclides in the body or…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2016

Medrad Source Administration Sets, Catalog number INT CSS. For use with MEDRAD Intego PET Infusion pump Systems, in…

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

Bayer Healthcare

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2016

Zimmer, Virage OCT Spinal Fixation System, Item Number: 07.01738.001, a posterior system intended to achieve an implant…

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

Zimmer Biomet, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 6, 2016

MOSAIQ Oncology Information System MOSAIQ is an oncology information system used to manage workflows for treatment…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW Etest¿ is a quantitative technique for…

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

Biomerieux

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

A.L.P.S. 4.0mm Cancellous Locking Screws intended for use in stabilization and fixation of fractures, revision…

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

Biomet, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Boston Scientific, Chariot ST-CCV Guiding Sheath, Sterilized using ethylene oxide: Product Description Material Number…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Optional PS500 Power Supply Unit for the Evita V500 Ventilator and Babylog VN500 Ventilator. Babylog VN500 is a…

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

Draeger Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Reagent Management System (RMS) Dimension EXL with LM Product Usage: The Reagent Management System (RMS) is a module…

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

Siemens Healthcare Diagnostics Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2015

MYLA CLINIC PATCH 3.2.0 CD Product Usage: MYLA is a computer application (Middleware) based on Web 2.0 technology…

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

bioMerieux, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2015

MOSAIQ Oncology Information System. Used to manage workflows for treatment planning and delivery.

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

Elekta, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 16, 2015

Red Bull Total Zero Energy Drink, 12 fl.oz. (355ml), UPC CODE(S): ON THE CAN: 6 11269 62373 4; ON THE CASE: 6 11269…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Red Bull North America Inc.

FDA (openFDA food enforcement)

Food

Reported Dec 9, 2015

Founders Pride Chocolate Chip Cookies 120 - 2.5 oz frozen dough pieces packaged per case, Net Wt. 18.75 lbs. (8.50 Kg.)…

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

Custom Foods Inc.

FDA (openFDA food enforcement)

Food

Reported Dec 9, 2015

Goodcents deli fresh subs Fresh Baked Giant Cookie, Chocolate Chip Cookie, Serving Size: 1 Cookie, Approx. NET WT. 2.5…

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

Mr Goodcents Inc.

FDA (openFDA food 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.