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 Dec 19, 2012
Berres Brothers Coffee Roasters Chocolate & Peanut Butter regular whole bean coffee packaged in the following sizes: 12…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Berres Brothers, Inc.
9 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 19, 2012
Reusable, non-sterile, self-adhering electrodes for use with TENS/NMES, . Made in the U.S.A. Cutaneous electrode is an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC dba Uni-Patch
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 19, 2012
The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that incorporates a high-resolution color camera, an…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Invivo Corporation Expression MRI Patient Monitoring System. The Expression MRI Patient Monitoring System is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Custom Procedural Trays: Merit's Custom Total Hip Pack, K12T-05537, Merit's Total Knee Pack, K12T05538 A custom…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Dec 12, 2012
The product has the Catalogue/Part number 60010. Olympic Cool-Cap System is a selective head cooling system for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Natus Medical Incorporated
FDA (openFDA device enforcement)
Reported Dec 12, 2012
Dimension Vista(R) IRON Flex(R) reagent cartridge (K3085) The IRON method is an in vitro diagnostic test for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 28, 2012
Styker Orthobiologics Vita Plasma Separator, a component of Vitagel Surgical Hemostat. Sterile, single use device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Orthobiologics, Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2012
PT Link Waterbath, Model#PT100. Lab Vision PT Module Plus provides an automated standarized alternative to labor…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dako North America Inc.
FDA (openFDA device enforcement)
Reported Oct 31, 2012
GE Seno Advantage 1.x, Seno Advantage 2.0, Seno Advantage 2.1 Seno Advantage 1.x, Seno Advantage 2.0, Seno Advantage…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2012
Hot Pepper Jelly, 4 and 8 ounce jars, labeled in part ***Jill's Jams & Jellies, Hampstead, MD 21074***
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hanover Pike Enterprises, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 24, 2012
Hemorrhoidal Circular Stapler and Accessories 33mm Product Usage: The PROXIMATE HCS Hemorrhoidal Circular Staplers,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Oct 17, 2012
Fresh Express Leafy Green Romaine; Crunchy Romaine Lettuce & Tender Green Leaf Lettuce 9 oz. bag, Keep refrigerated, no…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresh Express Incorporated
FDA (openFDA food enforcement)
Reported Oct 17, 2012
OrthoHelix Part #HCS-056-32 3.2MM Cannulated Hex Driver NON STERILE MAT: 465 SS The drivers are used to drive screws in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthohelix Surgical Designs Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 17, 2012
Battery, 100/115V (Includes charger and connecting cable) The Sarns" Centrifugal System is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 10, 2012
IR1200, IR1250(IR1200 Plus), 2020 and One Touch(R) Ping(R) Insulin Pump glucose management system. The device is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Animas Corporation
FDA (openFDA device enforcement)
Reported Oct 10, 2012
Optilock 2.7 mm Screw Inserter. Intended Use: The OptiLock Upper Extremity Plating System is intended for fixation of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 3, 2012
DEXIS Imaging Suite - catalog number 1.008.7932, version numbers 10.0.0 through 10.0.3 Radiological Image Processing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Imaging Sciences International, LLC
FDA (openFDA device enforcement)
Reported Oct 3, 2012
Invacare¿ I-Fit" Shower Chair (Models 9780, 9781, 9781-1), Invacare Corporation, Elyria, OH 44035. These shower chairs…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Oct 3, 2012
SharePlan 1.1, aka t-RayAutoplan version 1.2.1 (build number 1.3.1.10). Manufacturing name RayAutoplan, aka…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Oct 3, 2012
Fruit Mixes: 1) Dining In¿ Super Fruit Medley,10.5oz, UPC 1122508396, Use by date 9/6/2012; 2) Ready Pac¿ Super Fruit…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ready Pac Foods Inc.
11 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 3, 2012
Siemens Magnetom Skyra, Verio, Spectra and Biograph MMR Nuclear Magnetic Resonance Imaging System and Tomographic Imager
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2012
JUGGERKNOT IN¿GUIDE PUNCH, 2.9MM. The JuggerKnot 2.9mm In-Guide Punch is intended to be used to prepare a 2.9mm hole…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2012
Octopus 101 Perimeter; PeriTrend Software Analysis A perimeter is a device intended to determine the extent of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Haag-Streit USA Inc.
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.