All recall categories

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.

Food

Reported Aug 30, 2023

FANTA ZERO SUGAR orange 20 FL OZ (1.25 PT) 591 mL UPC 0 49000 04143 9 THE COCA-COLA COMPANY

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

RQA, Inc.

FDA (openFDA food enforcement)

Food

Reported Aug 23, 2023

Alpenfest Style Sachertote NET WT 17.6 OZ (1 LB 1.6OZ) 500g Frozen UPC:2010 0889 Packaged in Cardboard Carton.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Lidl US TRADING

FDA (openFDA food enforcement)

Food

Reported Aug 16, 2023

Caramel Butter Pecan Cup 14 fl oz. cup (8 per case) Paper cup with paper lid Brand: Eclipse Foods UPC: 810049270490…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Eclipse Foods Co.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 16, 2023

CD HORIZON Spinal System Solera Awl Tip Tap, REF NAV2006K

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Sofamor Danek USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 16, 2023

BURGER BUN WITH SEEDS 3507402 Flour, water, potato flour, eggs, sugar, shortening, milk powder, salt, yeast, S200 UPC…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Saffron Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 9, 2023

Impella RP Flex with SmartAssist intracardiac microaxial blood pump, Product Number 1000323

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Abiomed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 9, 2023

OEC Flexiview 8800 Systems with 9-inch Image Intensifier

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE OEC Medical Systems, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 9, 2023

VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs (VRT-AF)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Johnson & Johnson Surgical Vision, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 2, 2023

HAMILTON C1 Ventilator REF 161001 1610010 Is intended to provide positive pressure ventilatory support to adults and…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Hamilton Medical, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 2, 2023

FRED Flow Re-Direction Endoluminal Device, REF: FRED3507-PMA, FRED3511, FRED3511-PMA, FRED3516-CA, FRED3516-PMA,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Microvention Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 2, 2023

QIAstat-Dx¿ Respiratory SARS-CoV-2 Panel -IVD intended for the detection and differentiation of nucleic acid from…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Qiagen GmbH

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 26, 2023

Contour¿ next GEN Blood Glucose Monitoring System

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ascensia Diabetes Care US, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 26, 2023

Beckman Coulter DxA Automation System, DxA 5000, REF: B87352, IVD, 200240V, 16A, 50/60HZ, RxOnly

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Biomedical GmbH

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 26, 2023

RET Proximal Probe. Used in Fluorescence in situ hybridization (FISH), a laboratory technique for detecting and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cytocell Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 26, 2023

Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2, 61100; DUREPAIR DURA SUBSTITUTE 3 X 3, 61105;…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Neurosurgery

FDA (openFDA device enforcement)

Food

Reported Jul 26, 2023

Private Selection 48oz Classic Fruit Medley, frozen product, 8/48 oz bags per case. UPC 0 11110 82026 6. Distributed by…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Townsend Farms Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 19, 2023

HeartSine, REF: PAD-PAK-01, PAD-PAK-03 AND PAD-PAK-03j, CE0123 sold separately and with the HeartSine Samaritan Public…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

HeartSine Technologies Ltd.

FDA (openFDA device enforcement)

Food

Reported Jul 12, 2023

Gose con Sandia, Sour Ale with watermelon, limes and sea salt, 12 oz. Can 6 pk. (72 oz. total) Can UPC 7 96363 00495 2,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Avery Brewing Company

FDA (openFDA food enforcement)

Medical devices

Reported Jul 12, 2023

BD Synapsys Informatics Solution, Catalog Number 444150

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 12, 2023

BD Pyxis CII Safe, Software: V7, REF: 107-96, 107-97, 107-97-201; BD Pyxis CII Safe, Software: V7, REF: 107-223,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 12, 2023

da Vinci Xi/X Tip-Up Fenestrated Grasper, REF: 470347, VER: 12

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 12, 2023

Quidel Triage Cardiac Panel: REF: 97000HS, 97021HS (Troponin I), 97022HS (CK-MB and Troponin I), 97000HSEU,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Quidel Cardiovascular Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 12, 2023

Regal Gourmet Snacks Milk Chocolate Raisins 16oz. clear plastic tub, UPC 028744201002

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Regal Health Food International, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 12, 2023

Aptio Automation Storage and Retrieval Module (SRM)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

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Other states

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.