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 May 16, 2018

Raw Form Organics Maeng Da Kratom Emerald Green; 150 capsule and 300 capsule plastic bottles; Manufactured for Raw Form…

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

Triangle Pharmanaturals LLC

25 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 16, 2018

Lactosorb RapidFlap, bone plate, Model No. 915-0020 The RapidFlap LS Cranial Fixation System is indicated for use in…

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

Zimmer Biomet, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 9, 2018

Happy Harvest Leaf Spinach; Net Wt. 13.5 oz (383g); Ingredients: Spinach, Water, Salt. Distributed by Aldi Inc.…

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

Mccall Farms Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 9, 2018

Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Interventional fluoroscopic x-ray…

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

Philips Electronics North America Corporation

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

Accelerate PhenoTest BC kit, Ref #10101018. The firm name on the label is Accelerate Diagnostics, Tucson, AZ. A…

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

Accelerate Diagnostics Inc.

FDA (openFDA device enforcement)

Food

Reported May 2, 2018

Formagere de la Brie brand, l 'Explorateur, soft ripened cheese made from pasteurized milk, product comes in a 250g…

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

Cheezwhse/Com

FDA (openFDA food enforcement)

Medical devices

Reported May 2, 2018

clariti 1 day/Fresh Day 90 pack (-1.00), UV Blocking, 90 silicon hydrogel, daily disposable contact lenses The Clariti…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

CooperVision Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM, Product Number HEM3335, GTIN Number 1 -…

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

Covidien LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

Triathlon Revision Knee Catalog #5545-A-301 and Catalog #5546-A-601 The knee system devices are sterile, single-use…

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

Howmedica Osteonics Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported May 2, 2018

Shell Eggs packaged in quantities and styles of pack (plastic and pulp cartons, flats, and boxes)

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

Rose Acre Farm

FDA (openFDA food enforcement)

Food

Reported Apr 25, 2018

Kratom capsules labeled in the following ways: 1) Divinity Kratom 10 Capsule Dietary Supplement, Divinity Product LLC,…

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

Divinity Product Distribution LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 25, 2018

Human Fetal Hemoglobin (HBF-1) FITC Conjugate

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

Life Technologies Corporation

FDA (openFDA device enforcement)

Food

Reported Apr 25, 2018

Cali Green Malay Kratom all packages, all quantities

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

Nutrizone LLC

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 25, 2018

MEVATRON M2 / PRIMUS Mid-Energy, Digital Linear Accelerator, Model No. 01940035 Product Usage: The intended use of the…

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

Siemens Medical Solutions USA, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 25, 2018

SANTA CRUZ organic APRICOT fruit spread NET WT 9.5 OZ (270 g) UPC 0 36192 10514 8

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Smucker Natural Foods, Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 25, 2018

Zimmer Segmental System Proximal Femoral Component 38mm Offset, Model Number 00-5850-030-38 The Segmental System is…

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

Zimmer Biomet, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 18, 2018

Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults and pediatrics and optionally infants and…

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

Hamilton Medical AG

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 18, 2018

6.5" (17 cm) Smallbore Ext Set w/Remv MicroClave¿ Clear, NanoClave¿ T-Connector, Clamp, Rotating Luer, Bulk…

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

ICU Medical, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 18, 2018

AUTO REF/KERATOMETER ARK-1s

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

Nidek Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 11, 2018

HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual…

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

C.R. Bard, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 11, 2018

2008 K2 Hemodialysis Machine with software version 5.40, Models: (1) Hemodialysis SYS OLC/Diasafe PLS 190610, UDI…

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

Fresenius Medical Care Renal Therapies Group, LLC

FDA (openFDA device enforcement)

Food

Reported Apr 11, 2018

Coconut Smiles - Retail: International Harvest Brand Organic Go Smile! Dried Coconut Raw, in a 9 oz. poly/plastic bag,…

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

International Harvest, Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 11, 2018

King Arthur Flour, 100% Organic, Finely Ground, Coconut Flour, UPC 0 71012 10702 5, Distributed by: The King Arthur…

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

The King Arthur Flour Company, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 4, 2018

ARROW ENDURANCE" Extended Dwell Peripheral Catheter System, Catalog Numbers: EDC-00820 & EDC-00820-B

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

Arrow International 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.