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 1, 2019

MONARCH SOUTHERN BARBECUE SAUCE MADE WITH MUSTARD NET 128 FL OZ(1 GAL) 3.78L INGREDIENTS: WATER, HIGH FRUTOSE CORN…

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

The CF Sauer Company

FDA (openFDA food enforcement)

Medical devices

Reported May 1, 2019

Thoratec HeartMate 3 Coring Tool, Sterile EO, Rx Only, REF 10005872, an optional accessory of Thoratec HeartMate 3 Left…

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

Thoratec Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2019

Abbott Alinity i Processing Module LN 03R65-01 - Product Usage: The Alinity i processing module is a fully automated…

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

Abbott GmbH & Co. KG

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2019

FilmArray BCID Panel, IVD, Rx Only, BioFire Diagnostics, REF: RFIT-ASY-0126, and RFIT-ASY-0127, when used with the…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2019

Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for…

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

Cordis Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2019

Innova IGS 630, Angiographic X-Ray, s5i system option used in generating fluoroscopic and rotational images of human…

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

GE Healthcare, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 24, 2019

NadaMoo! Strawberry Cheesecake Non-Dairy Frozen-Dessert 16 ounce/pint packaged in a carton

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

Little Red Rooster Company

FDA (openFDA food enforcement)

Medical devices

Reported Apr 24, 2019

14F SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061422

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

Medical Components, Inc. dba MedComp

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2019

Acusnare Polypectomy (Duck Bill Shaped) Snare Used with an electrosurgical unit for endoscopic polypectomy.

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

Wilson-Cook Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 17, 2019

CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD), Pro. Code L20431 Product Usage: The affected CORAIL Neck Trials are…

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

DePuy Orthopaedics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 17, 2019

Exprt Precision System: Revision Hip, Proximal Body with Bolt, Lateral Offset, Sterile R, djo surgical, REF:…

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

Encore Medical, LP

FDA (openFDA device enforcement)

Medical devices

Reported Apr 17, 2019

syngo.via syngo.CT Cardiac Function, Model Number 10496180 Product Usage: Syngo.CT Cardiac Planning and syngo CT.…

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

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 10, 2019

McKesson Consult Diagnostic Immunochemical Fecal Occult Blood Test, Part numbers 178-CK30T, 178-CT30, 178¿TBSO,…

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

Cypress Medical Products LLC

FDA (openFDA device enforcement)

Food

Reported Apr 3, 2019

Jacques Big Daddy Dark Chocolate Bar. The product comes in un-coded 2.2 lbs. (1kg) clear plastic package overwrapped…

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

Jacques Torres Manufacturing , llc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 3, 2019

Paltop Premium Surgical Kit-containing the 1.25mm Hex Driver For surgical and restorative applications prosthetic…

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

Keystone Dental Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 3, 2019

Laparotomy Sponge with the following product description and model numbers: 1. Lap 18X18 XR (5 each/pack, 20 pack/case)…

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

Medical Action Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 27, 2019

Plain and Chromic Gut Absorbable Surgical Sutures, sterile. 12 sutures per box. Product Usage: Plain Gut Sutures are…

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

CP Medical Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 27, 2019

Ne-Mo's Chocolate Cake Square with Cream Cheese Icing, item 104; Net Wt. 3 oz. Case UPC: 2007606401046 4; Display pk 6…

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

Horizon Food Group

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 27, 2019

Lamb's Supreme Starz, item S0026, is formed star-shaped potato product that has been par-fried and frozen. Product is…

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

Lamb Weston Inc.

FDA (openFDA food enforcement)

Meat & poultry

Reported Mar 22, 2019

Two Brothers Pork Skins Retira productos de piel de cerdo debido a un error de rotulación y el incumplimiento del plan…

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

Two Brothers Pork Skins

USDA FSIS

Medical devices

Reported Mar 20, 2019

Cook Transseptal Needle, Reference Number TSNC-18-71.0, Order Number G02364. For transseptal left heart access in both…

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

Cook Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 20, 2019

Ossur Skull Pin, Sterile Titanium Pin, Part/Description: 516TS/ Skull Pin 2-1/4in TI Sterl 1PK; 516V2S/ Skull Pin 3in…

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

Ossur Americas

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 20, 2019

Simple Truth Organic Banana, Strawberry & Apple Fruit Puree with Nonfat Greek Yogurt, 113 g, packed in a laminate…

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

Perrigo Company PLC

FDA (openFDA food enforcement)

Medical devices

Reported Mar 20, 2019

AMSCO 3000 Series Washer/Disinfector Model # 3052

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

Steris 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.