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 48,784 notices were distributed nationwide, so they reach South Carolina too — those are in the archive.
Reported Jun 23, 2021
Ketamine HCl Injection Solution, 10 mg / 2 mL (5 mg/mL), Rx Only, Compounded by Prisma Health Outsourcing Facility 1071…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Prisma Health Outsourcing Facility
FDA (openFDA drug enforcement)
Reported Jun 23, 2021
Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 CPU is also used as spare part.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
Atec Insignia Anterior Cervical Plate System, REF 136-0116, Insignia, ACP, 1-Level, 16 mm, Rx Only, Non-Sterile, UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alphatec Spine, Inc.
28 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
DePuy Synthes Articul/eze Femoral Head: Hip joint metal/polymer semi-constrained cemented prosthesis. Part Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Jun 16, 2021
Ruffles All Dressed Potato Chips 16 1/8 oz. packaged in flexible plastic bags UPC 28400 56520
High riskUsing this product could cause serious injury, illness or death — stop using it now.Frito-Lay, Inc. Headquarters
FDA (openFDA food enforcement)
Reported Jun 16, 2021
Quickslide GramPro 1 Automated Gram Stanier is a microscope slide stainer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported Jun 16, 2021
Normand Remisol Advance Data Manager is a software device that interfaces between laboratory information systems (LIS)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Normand-Info S.A.S.U.
FDA (openFDA device enforcement)
Reported Jun 16, 2021
Ingenia Ambition X - Model Number: 781356, Diagnostic MR system. ***Updated November 2023*** Added Model Number 782109…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
1 more product in this recall
FDA (openFDA device enforcement)
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)
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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.