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 20, 2017
Rugby Calcionate Syrup, One Pint (473 mL)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Harvard Drug Group
16 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 13, 2017
MOSAIQ Medical Charged-Particle Radiation Therapy System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Sep 13, 2017
Southeastern Mills, Biscuit Gravy Mix, Net Wt. 2.75oz (77g), 4.5oz (128g) flexible plastic packages.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Southeastern Mills Custom Seasoning Solutions
5 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 13, 2017
JTS External Drive Unit JTS Distal Femoral Extendible Implant Femur is intended for the replacement of diseased or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stanmore Implants Worldwide Ltd.
FDA (openFDA device enforcement)
Reported Sep 6, 2017
UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System, Software Version 3.2. The DxH Slidemaker Stainer allows…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Sep 6, 2017
CORN TREATS CONCENTRATED CARAMEL CORN MIX NET WT 1 LB-6 OZ (22 OZ or 623 g) Manufactured by GOLD MEDAL PRODUCTS CO.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gold Medal Products Co.
FDA (openFDA food enforcement)
Reported Sep 6, 2017
iVue with Normative Database, Device Listing Number D185549. Product Usage: The iVue (K121739) is a non-contact, high…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Optovue, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 6, 2017
Toshiba America Medical Systems Ultimax Digital Fluoroscopic X-Ray System Model: DREX-UI80 Ultimax is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Aug 30, 2017
Gold Coast Packing Broccoli Florets; packed in the following configurations: 12 x 2 lb - Product code 508215 - Costco…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresh Venture Foods, LLC
FDA (openFDA food enforcement)
Reported Aug 30, 2017
DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation (DBS) lead kits, models 3387/3387S, 3389/3389S, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Aug 30, 2017
Medium Coated Jo-Jo Wedges / 00040 (5lb bags)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Penobscot McCrum LLC
9 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 23, 2017
Arctic Sun 5000 Temperature Management System, 100-120 V North America and 100-120 V US
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Aug 23, 2017
VNS Therapy¿ AspireHC¿ Generator, VNS Therapy¿ AspireSR¿ Generator. Model No. 105. Product Usage: United States…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cyberonics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 23, 2017
Truliant Tibial Trial Handle. To assist the surgeon in the implantation of Truliant Knee system components according to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Aug 16, 2017
iGUIDE Software 2.2 Product Usage: Control of accurate patient positioning with assistance of a 30 Tracking System in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Aug 9, 2017
GE Inspection Technologies Blade|line Industrial Cabinet X-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Inspection Technologies, LP
FDA (openFDA device enforcement)
Reported Aug 9, 2017
Professional Formulas Sublinqual B12 High-Potency dietary supplement, 60-count dissolvable tablet in white plastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Professional Complementary Health Formulas, LLC
FDA (openFDA food enforcement)
Reported Aug 9, 2017
InflammaDry(R) AN RPS DIAGNOSTIC SOLUTION, Sample Collectors InflammaDry(R) is a rapid, immunoassay test for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quidel Corporation
FDA (openFDA device enforcement)
Reported Aug 9, 2017
Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid Exchange Catheters Device is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
FDA (openFDA device enforcement)
Reported Aug 9, 2017
Lactulose Solution, USP, 10 g/15 mL, dose cups delivers 15 mL packaged in 50-unit dose cups per case, Manufactured by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.VistaPharm, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Aug 2, 2017
North Atlantic Brand - Approx8OZ Raw Breaded Swai Fillet - NET WT. 10lbs (4.54KG)
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Channel Fish Processing Co. Inc.
56 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 2, 2017
STOCKERT Heater-Cooler System 3T, 230 V
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group USA, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 26, 2017
Agfa Healthcare NX 3.0.8950 Imaging Processing Software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Healthcare Corp.
FDA (openFDA device enforcement)
Reported Jul 26, 2017
Penumbra 3D Revascularization Device It is indicated for used in the revascularization of patients with acute ischemic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Penumbra 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.