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 Aug 20, 2014

VIDAS D-Dimer Exclusion II, an automated quantitative test for use on instruments of the VIDAS family for the…

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

BioMerieux SA

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2014

Esaote PA230E Transducer A portable and cart base ultrasound system for general and cardiovascular imaging

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

Biosound Esaote, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2014

Codman Certas - In Line Valve Only; Product Code: 82-8800 The Codman Certas Programmable valve is an implantable device…

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

Codman & Shurtleff, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2014

EndoWrist Stapler System User Manual Addendum and Wall Chart; The EndoWrist Stapler 45 System and EndoWrist Stapler 45…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2014

Medtronic Ascenda Intrathecal Catheter models 8780 and 8781, and Ascenda Intrathecal Catheter Pump Segment Revision…

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2014

IntelliSpace Portal (ISP) DX/HX/EX, IntelliSpace Portal (ISP) IX, and IntelliSpace Portal (ISP) LX SPECT IntelliSpace…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 13, 2014

Sonopet Ultrasonic Surgical System Console, Ultrasonic Aspirator, Stryker Medtech.

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

Stryker Instruments Div.

FDA (openFDA device enforcement)

Food

Reported Aug 6, 2014

King of Pops Key Lime Pie, frozen flavored pop cycle, Net Wt. 3.2oz., Hand Made by King of Pops, 4845 Chateau Ave.,…

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

Coastal KOP LLC dba King

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 6, 2014

Horizon Medical Imaging It is a medical image and information management application that is intended to receive,…

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

Mckesson Medical Immaging

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2014

InTouch Critical Care Bed, Stryker Medical. Model Numbers 2130, 2131, 2140, 2141, 2151, 2152, 2155, and 2156.

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

Stryker Medical Division

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2014

Emerald Fiberoptic Blade, Macintosh 4, Teleflex Medical. A rigid laryngoscope is a device used to examine and visualize…

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)

Medical devices

Reported Aug 6, 2014

IPM Wound Gel Rx Wound Dressing IPM Wound Gel is indicated for the management of wound healing.

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

Wellspring Pharmaceutical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2014

AGFA Digital Radiography X-Ray system DX-D 100 Agfa's DX-D 100 is indicated for use in providing diagnostic quality…

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

AGFA Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2014

RECLAIM Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic Manual Surgical Instrument, used to ensure the…

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

DePuy Orthopaedics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2014

MK5 NX Controller--Wheelchair controller

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

Invacare Corporation

FDA (openFDA device enforcement)

Food

Reported Jul 30, 2014

Fat free cottage cheese sold under the Knudsen or Kraft brand and packaged in a plastic container with a net weight of…

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

Kraft Foods Group

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 30, 2014

Sarns D4 Aortic Arch Cannulae 6.0mm, 7mm & 8mm angled and straight tip with or without side holes and/or luer Product…

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

Terumo Cardiovascular Systems Corporation

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 23, 2014

ACL TOP (Base), automated coagulation laboratory instrument.

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

Instrumentation Laboratory Co.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 23, 2014

V-Series Patient Monitoring System, Manufactured for Mindray DS USA, Inc. Used for monitoring of human physiological…

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 Jul 23, 2014

H¿agen-Dazs Chocolate Chocolate Chip Ice Cream, 14 oz, UPC of 74570-08400

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

Nestle

FDA (openFDA food enforcement)

Food

Reported Jul 23, 2014

There are 2 different labels for this same product with the same UPC. Label #1 Individual Bars: 100% natural Zing…

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

NW Nutritional Foods LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 23, 2014

e.cam camera system. Emission Computed Tomography System used to detect or image the distribution of radionuclides in…

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

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 23, 2014

Vita Classic Premium Sliced Smoked Atlantic Nova Salmon, packaged in a black vacuum-sealed, plastic film package for…

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

Vita Food Products, Inc.

FDA (openFDA food enforcement)

Meat & poultry

Reported Jul 18, 2014

North Carolina Firm Recalls Grilled Chicken Product Due to Misbranding and Undeclared Allergen

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

North Carolina Firm

USDA FSIS

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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.