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.

Medical devices

Reported Feb 19, 2020

cobas infinity core, Material No. 7154003001. The device is a calculator/data processing module, for clinical use.

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 12, 2020

Bulk Pail Product -- Almark Foods HARD COOKED BROKEN EGG WHITES 20 LB pail, DIST BY: ALMARK FOODS, GAINESVILLE, GA…

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

Almark Foods, LLC

28 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 12, 2020

Cocoon Convective Warming System, Product Code: CWS4000 (110V).

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

Care Essentials Pty., Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2020

Reinforced Introducer Sets Maquet 7 Fr., Part Number: 0684 00 0403 06. It is an accessory to be used for percutaneous…

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

Datascope Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 12, 2020

Ducktrap River of Maine Herring Center Cuts in Wine Sauce, 12 oz.

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

Ducktrap River

FDA (openFDA food enforcement)

Food

Reported Feb 12, 2020

Garlic Parmesan Sauce; DP# 4478 FG# 02620 8/16 fl. oz (4.73 ml) pouches; NET WT. 8.05 lbs (3.65 kg) Produced for…

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

Golden State Foods

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 12, 2020

da Vinci Xi Surgical System Surgical System, IS4000, 00886874114216 - Product Usage: used with an endoscope, surgical…

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

Intuitive Surgical, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2020

Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob, 2264HAX, FFCM3205

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

Pacific Medical Group Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Feb 12, 2020

Ranitidine Hydrochloride (powder), USP, Rx only, Spectrum Chemical Mfg Corp., a) 1 gram, b) 5 grams, c) 25 grams, d)100…

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

Spectrum Laboratory Products

FDA (openFDA drug enforcement)

Food

Reported Feb 12, 2020

Fresh Location Protein Snack Tray 6.44oz, UPC: 8-5511000804-6

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

The H.T. Hackney Co. LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2020

Bard Conquest 40 PTA Dilation Catheter, 8mm X 20mm x 75cm (CQF7582), 8mm x 40mm x 75cm (CQF7584); Recommended Guidewire…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2020

GIBSON Healthcare Membrane 6-9, 15mm x 20mm, Reference Number 5303-226 - Product Usage: Indicated for use in oral…

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

Collagen Matrix Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2020

CS5/5+ Fastpacks, 225 mL, 150¿ Res Autotransfusion Device - Product Usage: its related accessory components are…

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

Haemonetics Corporation

21 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 5, 2020

Jeni's Dairy Free Cold Brew with Coconut Cream Pints frozen dessert

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

Jeni's Splendid Ice Creams LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2020

Healon GV PRO 0.85 mL, Model (U.S.): 10-2400-14, Model (O.U.S.): 10-2705-14, 10-2715-14, 10-2725-14, and 10-2755-14

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

Johnson & Johnson Surgical Vision Inc.

FDA (openFDA device enforcement)

Drugs

Reported Feb 5, 2020

Dimercaptopropanesulfonate Sodium (DMPS), Aqueous injection solution, 50mg/mL 5 mL SDV, Rx only, McGuff Compounding…

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

McGuff Compounding Pharmacy Services, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Feb 5, 2020

AQURE basic sytem, FLEXLINK, REF 933-599, Version: 2.3.3 (17), CE IVD, Rx Only, UDI: (01)05700699335999 Intended use:…

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Drugs

Reported Jan 29, 2020

Ranitidine, 150 mg Tablets, a) 7 count, b) 14 count, c) 20 count, d) 30 count, e) 60 count; Rx, Only, H.J. Harkins…

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

H J Harkins Company Inc. dba Pharma Pac

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 29, 2020

Paltop Dynamic Dental Implant Dia 3.25mm L 13.0 mm, Catalog Number 21-70020

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

Paltop Advanced Dental Solutions Ltd.

FDA (openFDA device enforcement)

Drugs

Reported Jan 29, 2020

Preferred Pharmaceuticals, Inc, Ranitidine Tablets, 150 mg, a) 30 count bottles (NDC: 68788-7388-3), b) 60 count…

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

Preferred Pharmaceuticals, Inc.

1 more product in this recall

FDA (openFDA drug enforcement)

Food

Reported Jan 29, 2020

Morrison's cornbread dressing packaged in 4lb tray

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

Savannah Food Company, Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 22, 2020

QuickDraw Venous Cannula, REF: QD22, UDI: 00690103182699; and REF: QD25, UDI: 00690103182705

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2020

LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an…

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

Physio-Control, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2020

ImplantDirect InterActive Precision IO Scan Adapter, Part #6534-09PT, Platform: 3.4mm, Non-Sterile, Rx. The firm name…

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

Implant Direct Sybron Manufacturing, LLC

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.