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.

3,219 stored notices name South Carolina, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach South Carolina too — those are in the archive.

Medical devices

Reported Feb 13, 2019

Henry Schein CU 1000 Halogen Curing Light, Catalog 900-4542. - Product Usage: Curing light for use in dentistry. The…

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

Handpiece Headquarters

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2019

Portex 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿

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

Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

12 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 13, 2019

Chicago's Pizza Base Mix, Manufactured Exclusively for Chicago's Pizza, Greenfield, IN packaged in 30 lb bags.

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

Pizza Blends, LLC

9 more products in this recall

FDA (openFDA food enforcement)

Meat & poultry

Reported Feb 10, 2019

VICS Acquisition, LLC retira productos de pollo debido a un error de rotulación y alérgenos no declarados

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

VICS Acquisition, LLC

USDA FSIS

Food

Reported Feb 6, 2019

LUNCH BOX SANDWICHES HAM & CHEESE CROISSANT; NET WT 5OZ (142G); MADE BY: GS Sandwich Co. Longs, SC 29568 843.399.2999;…

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

Grand Strand Sandwich Company,Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 6, 2019

Cell Saver 5/5+ Bowl Set, 70ml, Product ID: 0291E-00, 0291A-00 Indications for Use: The Haemonetics Cell Saver 5/5+…

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

Haemonetics Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 6, 2019

Peaches, sold as a bulk retail item, with PLU 4044, and country of origin of Chile. The peaches sold at Aldi are…

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

Jac Vandenberg Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 30, 2019

Del Monte Quality Fresh Cut Harvest Selects Fiesta Corn seasoned with Red & Green Peppers. NET WT 15.25 oz. (432 g);…

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

Del Monte Research Center - Walnut Creek

FDA (openFDA food enforcement)

Medical devices

Reported Jan 30, 2019

VentStar Basic 180, Catalog Number MP00349 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit…

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

Draeger Medical, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 30, 2019

Perfusion Pack, Rx only, Sterile EO

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

LivaNova USA

FDA (openFDA device enforcement)

Medical devices

Reported Jan 23, 2019

Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anchor pre-loaded on a handled inserter including suture, with…

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

Arthrex, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 23, 2019

U by Kotex¿ Sleek¿, Regular Tampons, 18 Count

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

Kimberly-Clark Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 23, 2019

PREMIER Cryptococcal Antigen, Catalog Number 602096 Product Usage: The PREMIER Cryptococcal Antigen enzyme immunoassay…

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

Meridian Bioscience Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 16, 2019

DX-D 600 DIRECT RADIOGRAPHY SYSTEM Product Usage: The DX-D 600 system is a ceiling mounted General Radiography X-Ray…

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

Agfa-Gevaert, N.V.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 16, 2019

Various GE Magnetic Resonance System on-site software version Product Usage: Magnetic resonance imaging equipment for…

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

GE Healthcare, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 9, 2019

StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation Cranial Optical Pocket Guide - Instructions for…

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 9, 2019

Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Dose 200pk Cool Mint: Enamelast 5% Sodium Fluoride Unit…

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

Ultradent Products, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2019

HydroSet XT Injectable HA Bone Cement, REF 897003, STERILE

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

Howmedica Osteonics Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2019

Thermoset Room Temperature Closed Loop Injectate Delivery System. 1 unit per Cavity #3 Cavity Deep/20 pieces per case…

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

ICU Medical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2019

Medtronic MiniMed 630G 6025805-003_C, Rx Only Medtronic MiniMed 670G 6025805-005_B, Rx Only Medtronic MiniMed 640G…

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

Medtronic Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 26, 2018

Wegmans Roasted Corn and Bean Salad; 13 oz. Plastic Container, 40 oz. Plastic Container, 4.5 lb. Plastic Bulk Container

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

ASK Foods Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 26, 2018

Baked Macaroni and Cheese, NET WT 12 OZ (340g), CONTAINS: WHEAT, MILK, EGG, Produced By BAKKAVOR USA, 2700 Westinghouse…

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

Bakkavor Foods USA Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 26, 2018

enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated for primary implantation for the visual…

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

Bausch & Lomb Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 26, 2018

VITEK 2 Antimicrobial Susceptibility Testing (AST) using one or more of these susceptibility products: Catalog #…

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

bioMerieux, Inc.

1 more product in this recall

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.