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.
3,275 stored notices name South Carolina, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,828 notices were distributed nationwide, so they reach South Carolina too — those are in the archive.
Reported Jan 18, 2017
Cardboard sleeve: Double Takes Macaroni & Cheese Dinner, Distributed By: Greenbrier International, Inc., 500 Volvo…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fourth Street Barbeque, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 18, 2017
OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2017
House Autry, stone Ground Buttermilk Corn Bread Mix, Net wt. 8 oz. boxes, UPC Code 0 73484 15512 2,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.House-Autry Mills, Inc.
6 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 18, 2017
Merge Eye Station f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Tropical Fruit Supreme, packaged under the following brands: (a) St. Clair, product code 104001, ST. CLAIR FOODS, INC.,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.St Clair Foods, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 18, 2017
Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT, CR3434CT Ablation catheter cables are designed as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Non Fat Dry Milk, Grade A - High Heat in 50 # bags , manufactured by Valley Milk Products. Stasburg, Virginia 22657 ,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Valley Milk Products
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 18, 2017
VOCO Futurabond M+ adhesive, RF 1515, Manufactured by VOCO GmbH, Futurabond M+ is a dental adhesive for use with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Voco GmbH
FDA (openFDA device enforcement)
Reported Jan 11, 2017
Carolina Moon, typical wheel is about .55 lb, Chapel Hill Creamery, Chapel Hill, NC 27516, sold by weight.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Chapel Hill CreameryLLC
12 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 11, 2017
Wal-Mart, Marketside Veggie Kabobs 23oz
High riskUsing this product could cause serious injury, illness or death — stop using it now.Country Fresh Products, LLC
21 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 11, 2017
AMERICAN CLASSIC SUB Net Wt 6.5 oz (184g) Smoked ham, deli style bologna, hard salami with American and Swiss cheese on…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eby Brown Co.
9 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 11, 2017
G3 Opticage Expandable Interbody Fusion Device, Model No. 9180-00, 9180-01, 9180-06, 9180-07, 9180-17, 9101-00, 9101-06…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Interventional Spine Inc.
FDA (openFDA device enforcement)
Reported Jan 4, 2017
Innova 2000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 4, 2017
Specimen Gate Laboratory 5002-0180, Specimen Gate eReports 5002-0370, Software Version 1.0 Specimen Gate Laboratory is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PerkinElmer Health Sciences, Inc.
FDA (openFDA device enforcement)
Reported Jan 4, 2017
Publix Premium Banana-Flavored Chocolate Chip Pancake & Waffle Mix, 16 oz box.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Publix Super Markets, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 4, 2017
Shimadzu X-ray TV System, Catalog No. SONIALVISION G4
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 4, 2017
SOMATOM Scope, Computed tomography x-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Zeus-P Lumbar Interbody Device
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amendia, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Micro-Introducer Kit, 45CM SS/SS…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Angiodynamics, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath¿…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Fresh Express Kit Caesar salad, Net Wt. 7.6 oz. (215g), Fresh Express Incorporated, 550 S. Caldwell St. Charlotte, NC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresh Express Incorpated
FDA (openFDA food enforcement)
Reported Dec 28, 2016
Rx CHOICE brand LIQUID VITAMIN C, 16 FL OZ (473 mL), NDC 50383-167-16 --- HI-TECH PHARMACAL CO., INC. Amityville, NY…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hi-Tech Pharmacal Co., Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 28, 2016
Merge OrthoCase software. The firm name on the label is Merge Healthcare, Hartland, WI.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, 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.