All recall categories

Recalls distributed in North Carolina

These notices name North 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.

4,689 stored notices name North Carolina, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,123 notices were distributed nationwide, so they reach North Carolina too — those are in the archive.

Food

Reported Dec 19, 2018

Imperial Taste Fried Red Onion, Cu Hanh Phi; 24 x 8oz. Item #1760, UPC Code: 741861017607; 24 x 12oz. Item #1761, UPC…

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

Gemini Food Corporation Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 19, 2018

Medtronic HeartWare Ventricular Assist HVAD System Battery Charger Model 1600US - Product Usage: The HeartWare…

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

Heartware, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 19, 2018

UroLift System REF Catalog Number: UL400-4 Tray Contents: UroLift System with Handle Release Tool STERILE R CE 0050…

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

Neotract Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 19, 2018

HeartStart MRx, Rechargeable Li-Ion (lithium ion battery), REF: M3538A, which is a component of HeartStart MRx…

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 19, 2018

St. Jude Medical InfinityTM DBS System 8CH Directional Lead, 30 cm, 0.5 REF 6170 - STERILE EO Rx ONLY CE 0086 0123 St.…

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

St. Jude Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 12, 2018

BD BBL Trypticase Soy Agar with 5% Sheep Blood, Catalog No. 221261, (non-selective, non-differential)

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 12, 2018

Captus 3000 Thyroid Uptake System, Model # 5430-0076 and 5430-0077

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

Capintec Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 12, 2018

16 count Smartfood Delight Variety Pack Sack

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

Frito-Lay, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 12, 2018

NOW Vitamin B-50 Complex with C 100 Veg Caps

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

NOW Foods

FDA (openFDA food enforcement)

Food

Reported Dec 12, 2018

Smartypants Kids Complete, Non GMO Multi and omega 3's vitamin D3 for bones, vitamin B12 for Energy: 90 gummies. UPC 8…

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

Smartypants Vitamins

FDA (openFDA food enforcement)

Medical devices

Reported Dec 5, 2018

QUADROX-i Neonatal without integrated arterial filter and VHK 11000 (VKMO 10000-USA#QUADROX-i Neo.+Reservoir), Part…

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

Maquet Cardiovascular US Sales, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2018

The SQ-RX Pulse Generator a component of the Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System The…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Food

Reported Nov 28, 2018

HOUSE BLEND Barbecue SAUCE INGREDIENTS: ***Contains 2% or less of Soybean Oil***Onion Powder***Calcium Disodium…

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

Diamond Crystal Brands, Inc.

FDA (openFDA food enforcement)

Food

Reported Nov 28, 2018

Mast Store Provisioners, Dried Okra, Net Wt. 4 OZ. clear plastic bag

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

Lehi Valley Trading Co.

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 28, 2018

Irrisept OR, Finished Bottle Assembly 450 ml STEP 1

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

Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2018

Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 (Model: Minicon…

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

Merck Millipore Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2018

Binding Site Human IgM Kit (for SPAPLUS), REF: NK012.S The device consists of reaction buffer, sheep anti-IgM…

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

The Binding Site Group, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

Arrow AGB+ Multi-Lumen CVC Kit, 7 Fr., 3 Lumen, 20cm catheter length, .025 inch dia. spring-wire guide, Product Code…

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

Arrow International Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

3.2mm Proximal Reamer/Cannulated Drill provided as part of the Fibulock Fibular Nail System Pack. FibuLock Nail…

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

Arthrex, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

bioM¿rieux NucliSENS easyMAG Lysis Buffer ref. 280134

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

bioMerieux, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

Espiner Tissue Retrieval System-Eco-Sac Trocar 12mm Vol: 1200 ml EMP160ECO-US-5 (GTIN:5060358120367) Product Usage:…

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

Espiner Medical Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

GE Healthcare Millennium MyoSIGHT Nuclear Cardiology Imaging System H3000ZH Acquisition System

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

GE Healthcare, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

Abbott TECNIS 1-Piece Aspheric Acrylic IOL with the TECNIS iTEC Preloaded Delivery System, Lens Model PCB00, Sterile,…

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

Johnson & Johnson Surgical Vision Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as five-pack carriers) Product Usage: In vitro…

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

Luminex Corporation

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.