All recall categories

Recalls distributed in South Carolina

These notices name South Carolina 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.

3,277 stored notices name South Carolina, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,842 notices were distributed nationwide, so they reach South Carolina too — those are in the archive.

Medical devices

Reported Nov 7, 2012

HeartSine Samaritan(R) 300/300P PAD devices with serial numbers 0400000501 to 0700032917; 08A00035000 to 10A0070753;…

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

Heartsine Technologies, Limited

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2012

Oncentra External Beam 4.1. Radiation treatment planning software designed to analyze and plan radiation treatments in…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2012

Gish 3/8 x 3/8" Straight Connector with Luer fitting, Item Numbers: EC2160B, EC2160S, Lot Numbers: 1210100010,…

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

Sorin Group USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2012

Perfusion System 8000, base 4 pump, 115V safety monitor included The Sarns Modular Perfusion System 8000 is indicated…

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

Terumo Cardiovascular Systems Corporation

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

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)

Food

Reported Oct 24, 2012

Kilwins Sugar Free S/F PEANUT BUTTER FUDGE, Nt. Wt. 7-oz (198 g)

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

Kilwin's Quality Confections, Inc.

FDA (openFDA food enforcement)

Food

Reported Oct 24, 2012

***Publix***Hearts of Romaine***Chopped Hearts of Romaine***Triple Washed***& Ready to Eat***No Preservatives***NET WT…

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

Publix Super Markets

FDA (openFDA food enforcement)

Medical devices

Reported Oct 24, 2012

Helion and Xenion surgical lights, 501/01 series KLM lights. The surgical lights are intended to locally illuminate an…

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

Trumpf Medical Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 17, 2012

Maryland Crab Cake Bulk (fresh), #81868, 4oz @2x8ct, Net Wt. 4 lbs, Packed by 3fish, Inc.

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

3fish Inc.

11 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 17, 2012

3M Steri-Vac Gas Sterilizer/Aerator models 5XL and 8XL. 3M Steri-Vac Gas Sterilizer/Aerator is a compact unit designed…

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

3M Company - Health Care Business

FDA (openFDA device enforcement)

Medical devices

Reported Oct 17, 2012

PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation…

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

Biomerieux Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 17, 2012

FRESH SELECTIONS by Kroger" Tender Spinach NET WT 10 OZ (283g) BEST IF USED BY 09/16/12 Product of USA 10:09…

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

Kroger Co.

FDA (openFDA food enforcement)

Medical devices

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)

Medical devices

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)

Food

Reported Oct 10, 2012

Coast Tropical Brand Whole Mangoes, Kent & Keitt's varieties, 10 lb box. The recalled mangos were sold between July 7,…

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

Coast Citrus Dist

FDA (openFDA food enforcement)

Medical devices

Reported Oct 10, 2012

BriteField illuminated Suction Device; Model numbers 8Fr, 10Fr and 12Fr, Kit (included 8Fr, 10Fr and 12Fr and a…

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

Invuity, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 10, 2012

Endoscopic retrieval device. The disposable Raptor grasping device in intended to retrieve foreign bodies or resected…

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

US Endoscopy Group Inc.

FDA (openFDA device enforcement)

Medical devices

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)

Medical devices

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)

Food

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)

Medical devices

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)

Medical devices

Reported Sep 26, 2012

Precise Digital Accelerator Delivery of radiation to defined target volumes

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

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)

Medical devices

Reported Sep 26, 2012

The 2.7mm Drilling Guide is a reusable instrument used in conjunction with a drill to prepare oriented holes in bone…

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

Integra Life Sci.

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.