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 48,122 notices were distributed nationwide, so they reach South Carolina too — those are in the archive.
Reported Sep 2, 2015
ExacTrac 6.0.x Patient Positioning System, Radiation therapy. Intended to be used to place patients at an accurately…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Sep 2, 2015
cobas b 123 Fluid Pack COOX REF 05169992001 200 Product Usage: The cobas b 123 POC system is a fully automated POC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2015
Kroger Ground Cinnamon UPC 11110 70034 NEW WT. 18.3 oz Plastic container
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 2, 2015
3.0/4.0 Cannulated Drill Bit; a component of the Tiger Cannulated Screw System The Tiger Cannulated Screw Fixation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical Ltd.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 10 Fr, (30/box), Product Code 51610. Intermittent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Alaris Medley LVP Frame Membrane. Intended use to hold platen assembly and help protect the bezel assembly's internal…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Elite Biomedical Solutions LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Frozen Jamba, Fruit & Veggie Smoothies, Green Fusion, Green Apple, Mango, Pineapple, Kiwi, Banana, Broccoli and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Inventure Foods
64 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 26, 2015
Siemens Symbia S Series system, a diagnostic analog or digital detector based planar (2- dimensional) nuclear medicine…
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 Aug 26, 2015
Stryker Orthopaedics Triathlon X3 Tibial Bearing Insert - CR REF 5530-G-209 (component of the Triathlon Total Knee…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Howmedica Osteonics Corp.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Bronchial Double Lumen Tube Set (Left), Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and 3.0/4.0 Cannulated Screw Countersink Part #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical Ltd.
FDA (openFDA device enforcement)
Reported Aug 19, 2015
Oasis Coil Extension Cable used with Hitachi Oasis MRI System Product Usage: The Oasis MR system is an imaging device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Aug 19, 2015
Invacare¿ Pronto¿ Air Personal Transporter (power wheelchair), Invacare Corporation, One Invacare Way, Elyria, Ohio,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Aug 12, 2015
Merge Hemo, 9.10, 9.20.0, 9.20.1,9.20.2, 9.30, 9.40.0, 9.40.1, 9.40.2 with Massimo PHASEIN End Tidal CO2 (EtCO2)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Aug 12, 2015
Wish-Bone Ranch Dressing Net. Wt. 24 oz. Distributed by Pinnacle Foods Group USA LLC Cherry Hill, NJ 08003-3620 UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pinnacle Foods, LLC
FDA (openFDA food enforcement)
Reported Aug 12, 2015
S2 Fluid Pack on the Cobas b 221 system- Catalog Number 03260925184 Blood Gas and Electrolytes Analyzer; The Roche…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Aug 12, 2015
18inch Dual Port/Single Bladder Disposable Tourniquet Cuff, Zimmer Surgical, Inc. Tourniquets are intended to be used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2015
Atkins Chocolate Candies 5 ct. cartons - UPC code 637480075558
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atkins Indiana Distribution Center
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 5, 2015
Fat Free Pasteurized Prepared Cheese Product: SOUTHHOME 12/12OZ AMERICAN FAT FREE YELLOW, 0788001319. ROUNDYS 12/12OZ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dairy Farmers OF America Inc.
33 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 5, 2015
IPS Empress Universal Glaze Spray 270 mL, Product Code/Model/Catalog Number 609432AN, Rx only. Porcelain glaze spray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ivoclar Vivadent, Inc.
FDA (openFDA device enforcement)
Reported Aug 5, 2015
Paragon Laboratory Management
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McKesson Technologies, Inc.
FDA (openFDA device enforcement)
Reported Aug 5, 2015
Invivo Expression MRI Patient Monitoring System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported Aug 5, 2015
Computed Tomography X-ray Systems Brilliance CT 64-channel with Essence technology. Intended to produce cross-sectional…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
American Catheter / Cholangiogram Catheter 9100 Series.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Catheter Corp.
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.