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.

3,275 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.

Medical devices

Reported Jan 12, 2022

Simplexa Direct Amplification Disc Kit, Product Kit Code MOL1455

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

DiaSorin Molecular LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 5, 2022

iDesign, Model - G300: System AWS (International), System AWS (China), Advanced WaveScan Studio (United States);…

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

AMO Manufacturing USA, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 5, 2022

RAPID 20 E, REF 20701, System for the identification of Enterobacteriaceae in 4 hours, 25 strips/package, IVD.

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

Biomerieux Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 5, 2022

Karl Storz Udel Sterilization Tray Instructions for Use, Tray Part Number/Description: 39301ACTS/CAMERA TRAY (STERRAD,…

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Jan 5, 2022

ARTISTE with syngo RT Therapist-linear accelerator systems to deliver X-Ray photon and electron radiation for the…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

TruDi NAV Suction Instruments: 0-Degree, REF: TDNS000Z; 70-Degree, REF: TDNS070Z; and 90-Degree, REF: TDNS090Z

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

Acclarent, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

SYNCHRON Systems Cholesterol (CHOL) Reagent, REF: 467825

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

WIRION EMBOLIC PROTECTION SYSTEM, Delivery Catheter and Filter and Retrieval Catheter, 6Fr, REF (Model Number) WRN-D6

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

Cardiovascular Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

Stealthstation System w/ Stealthstation Cranial Software 3.1.1,3.1.2,3.1. or SynergyCranial Software. Synergy Cranial,…

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

Medtronic Navigation, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw, Model #41122718, 2.7mm x 18mm, a component of the CHARLOTTE…

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

Wright Medical Technology, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

Box Label: activ5 TINY GYM IN YOUR POCKET activbody Model: Activ5 User Manual: ACTIV5 USER MANUAL Welcome to Activ5,…

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

Activbody, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 22, 2021

Krispy Kreme DOUGHNUT Bites ORIGINAL GLAZED 5 1.6 OZ (45g) POUCHES NET WT. 8 OZ (227g) Manufactured under the authority…

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

Krispy Kreme Doughnut Corporatio

FDA (openFDA food enforcement)

Medical devices

Reported Dec 22, 2021

MENTOR Saline-Filled Breast Implants are constructed from room temperature vulcanized silicone elastomer, made of…

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

Mentor Texas, LP.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

Miami J Select Collar, Item: MJS-101, and Miami J Select Collar Set, Item: MJSR-101 Instructions for Use

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

Ossur Americas

FDA (openFDA device enforcement)

Medical devices

Reported Dec 15, 2021

SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE BIOPSY INSTR 14GA X 9CM; 701114150/SUPERCORE…

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

Argon Medical Devices, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 15, 2021

OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 REF 450-0021-00 -OsteoMed D-Power Control…

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

Osteomed, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 15, 2021

TaDah! FALAFEL STREET WRAP WITH SPICY BROWN SUGAR HARISSA HUMMUS NET WT. 7.5 OZ. UPC Code:8-5019800307-5

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

The Fillo Factory Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 8, 2021

BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147 UDI: 00815381020338 Blood Culture Catalog…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

SHIP KIT, PROCEDURE KIT, PROTEKDUO LS - DL31 for temporary Cardiopulmonary bypass. Including the following components:…

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

Cardiac Assist, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 8, 2021

Tastykake Buttercreme Iced Creme Filled Chocolate Cupcakes 14.25oz (6-2ct) box UPC 0 25600 00230 8 & 2.375oz package,…

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

Flowers Foods (Corporate Offices)

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 8, 2021

GE Centricity Universal Viewer Zero Footprint Client

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

The Steripath Gen2 Blood Collection System Model Number/Description 2700-21-EN / Steripath Gen2 Blood Collection System…

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

Magnolia Medical Technologies, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Number/Product…

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

NuVasive Specialized Orthopedics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

Abbott HeartMate Touch Communication System, REF: HMT1100 (US), HMT1100-R (Rental US), HMT1150 (EU)

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

Thoratec Corp.

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.