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.
Reported Mar 4, 2015
The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare…
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)
Reported Mar 4, 2015
TDX Electric Wheelchair. Invacare FDX, TDX series and Storm Series (3G) power wheelchairs in 20 to 24 inch width…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 4, 2015
CoCr Femoral Head - A modular head component is used in conjunction with a femoral stem component for replacement of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer GmbH
4 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 18, 2015
Amana Dinner Rolls, packaged in 1 lb 2 oz plastic bags
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Jefferson Street Bakery Inc.
FDA (openFDA food enforcement)
Reported Feb 11, 2015
SoftLab with SA HIS versions 4.0.7.0-4.0.7.1 SoftLab is a laboratory information system to be used in a medical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SCC Soft Computer
FDA (openFDA device enforcement)
Reported Jan 28, 2015
Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Jan 28, 2015
PF4 Concentrated Wash (10x), REF 403624, packaged in the following assay kits: 1. ImmucorGamma LIFECODES PF4 IgG…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Genetic Testing Institute,Inc.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
iPlan RT Dose is a stereotactic radiation treatment planning system that is intended for use in stereotactic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Philips Expression MR200 MRI Patient Monitoring System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Jan 21, 2015
The SurgiCounter Charging Cradle Product Usage: SurgiCounter Charging Cradles are designed to be used with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Jan 14, 2015
Abdallah Milk Chocolate Bites CARAMEL, Net Wt 4.5 oz. (127g), UPC 7 6668407116 2, Ingredients: Pure milk chocolate…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abdallah Candies, Inc.
FDA (openFDA food enforcement)
Reported Dec 24, 2014
Additional devices identified in new FSN MA-FCO 83000190: QLAB versions 10.0 with a2DQ and/or aCMQ plug-ins installed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Crocodile (size 3) are two-armed, wheeled walking aids, used by children with disabilities. Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Snug Seat Inc.
FDA (openFDA device enforcement)
Reported Dec 17, 2014
TomoTherapy Treatment System with software versions 2.0.1 / 2.0.2 / 2.0.3/ (Hi:Art 5.0.1 / 5.0.2 / 5.0.3)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TomoTherapy Incorporated
FDA (openFDA device enforcement)
Reported Dec 10, 2014
Amerigel Hydrogel Wound Dressing Wound management
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerx Health Care Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 10, 2014
MAS CardioImmune XL Cardiac Marker Control; Model: CAI-XL1; intended for use in the clinical laboratory as an assayed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microgenics Corporation
FDA (openFDA device enforcement)
Reported Dec 10, 2014
Aquapak Adaptor, 028 NEB, INTL, Product No. 403128; Aquapak Adaptor, 033 NEB, INTL, Product No. 403133; Aqaupak…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2014
ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 or 4 Bottle(s) (6.6 mL/27.0 mL) anti-T3 (sheep) coated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
FDA (openFDA device enforcement)
Reported Dec 3, 2014
Karlsburger Foods Taco Seasoning, Item Numbers 43823 (Packaged in 23 oz resealable plastic containers), Item #43807…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Karlsburger Foods, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 3, 2014
Remel TB Potassium Permanganate (.5% Aqueous) 40192, packaged in 250 ml bottles, 5/pkg. A stain for use in qualitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 26, 2014
Edwards Lifesciences Vent Catheters, . Packaged sterile and non-pyrogenic in a sealed, peel-type pouch. Model Numbers:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Nov 19, 2014
Rapid Neg BP Combo Panel Type 3; Catalog number B 1017-117. MicroScan Rapid panels are designed for use in determining…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 19, 2014
The 5085 is a general surgical table with high patient weight capacity, extended width capability, and lower minimal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Nov 5, 2014
DMI Duro-Med Industries Rollator Transport Chair; Wheel Size: 7 1/4"; Overall Width: 23 1/2"; Seat Height: 21 1/4";…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Briggs Medical Service Company d.b.a. Mabis
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.