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.
Reported Jun 16, 2021
RayStation (Treatment Planning System) Model Number RayStation is 6.0.0.24 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 ,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jun 9, 2021
NexSite HD, Hemodialysis Symmetric Tip Catheter for long term use
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Marvao Medical Devices Ltd.
FDA (openFDA device enforcement)
Reported Jun 2, 2021
THERAPEUTIC M 130; NDC/UPC 740985223680; OTC; TABLETS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health Inc.
197 more products in this recall
FDA (openFDA drug enforcement)
Reported Jun 2, 2021
IRON GEN 2: ROCHE COBAS INTEGRA ANALYZER, REAGENT CASSETTES, Catalog#: 03183696122 - Product Usage: In vitro test for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported May 26, 2021
ISOMORPH 28 PURE WHEY iSOLATE BANANA CREAM PIE DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89846 7 & 5LB, UPC 6 49241…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hi Tech Pharmaceuticals
13 more products in this recall
FDA (openFDA food enforcement)
Reported May 26, 2021
PUBLIC GOODS brand HAIR, SKIN, & NAILS Dietary Supplement; 60 tablets per bottle; Other ingredients: Stearic acid;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Public Goods
FDA (openFDA food enforcement)
Reported May 26, 2021
Elecsys Troponin I STAT Immunoassay: Catalog# 05094798160 - Product Usage: intended to aid in the diagnosis of…
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 May 26, 2021
Alpha Interlock Suspension System Lanyard Body: An external prosthetic device. The Alpha Lanyard includes suction with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.WillowWood Global LLC
FDA (openFDA device enforcement)
Reported May 19, 2021
Provox Life Night HME, Catalogue Number 8262 - Product Usage: single use heat and moisture exchangers for patients…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atos Medical AB
FDA (openFDA device enforcement)
Reported May 19, 2021
PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 19, 2021
AquaBplus and AquaBplus B2 Water Purification System - Product Usage: Intended for use with a hemodialysis system to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Holdings, Inc.
FDA (openFDA device enforcement)
Reported May 19, 2021
ASSURITY Pulse Generator REF PM**** SN ********* ST. JUDE MEDICAL Assurity and Endurity pacemakers are intended to…
High riskUsing this product could cause serious injury, illness or death — stop using it now.St. Jude Medical, Cardian Rhythm Management Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 12, 2021
Centricity Universal Viewer - Product Usage: intended to assist in the viewing, analysis, diagnostic interpretation,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported May 12, 2021
VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greiner Bio-One North America, Inc.
FDA (openFDA device enforcement)
Reported May 12, 2021
Grace Medical REF S-2500 *** SHEEHY BONE DUST COLLECTOR *** Stainless steel filter - Product Usage: intended to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oto Med Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 12, 2021
Velvet Buckeye Classic 16oz - 8 cartons to a case 56oz - 4 cartons to a case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Velvet Ice Cream Company
55 more products in this recall
FDA (openFDA food enforcement)
Reported May 5, 2021
Spectrum IQ - Infusion Pump - Product Usage: intended to be used for the controlled administration of fluids.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported May 5, 2021
Stryker Medela REF 077.0193 AXS Universal Aspiration Tubing (01)07612367053921 - Product Usage: AXS Universal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medela AG Medical Technology
FDA (openFDA device enforcement)
Reported May 5, 2021
Power Wheelchair
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merits Holdings Co. dba Merits Health Products, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 5, 2021
InCore Lapidus Disposable Kit 28mm Left, Part Number: IC-LAP-28L - Product Usage: Intended as a three-part construct…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nextremity Solutions
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 5, 2021
VITROS¿ Black Reference Slides CATALOG #: J02316 - Product Usage: The Black Reference Slide is a part/ tool used in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported May 5, 2021
Dark Chocolate Expresso Beans; Net Wt. 12 oz. (340g), Best if used by 11-19-2021. Contains Soy, May Contain Milk.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Torn & Glasser, Inc.
FDA (openFDA food enforcement)
Reported Apr 28, 2021
Smart Port CT-Implantable Port Catalogue #: CT96STSD-VI, CT96STSA-VI - Product Usage: indicated for any patient…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics Inc. (Navilyst Medical Inc.)
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 21, 2021
MAMBA Flex 135 Microcatheter. Packaged with protective sleeve over catheter, sealed in a Tyvek pouch, and is then…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
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.