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 48,122 notices were distributed nationwide, so they reach North Carolina too — those are in the archive.

Food

Reported Sep 13, 2017

Southeastern Mills, Biscuit Gravy Mix, Net Wt. 2.75oz (77g), 4.5oz (128g) flexible plastic packages.

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

Southeastern Mills Custom Seasoning Solutions

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 6, 2017

UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System, Software Version 3.2. The DxH Slidemaker Stainer allows…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 6, 2017

HEALTH WARRIOR CHIA BAR ACAI BERRY NT WT 25 g (.88 g) ALLERGENS: Contains Tree Nuts (Cashews)

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

Belmont Confections Inc.

6 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 6, 2017

CORN TREATS CONCENTRATED CARAMEL CORN MIX NET WT 1 LB-6 OZ (22 OZ or 623 g) Manufactured by GOLD MEDAL PRODUCTS CO.

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

Gold Medal Products Co.

FDA (openFDA food enforcement)

Food

Reported Sep 6, 2017

Mary's Gone Crackers Original Crackers: Organic, Gluten Free, Non-GMO, Vegan. 6.5 oz. (184 g) box; Ingredients: Whole…

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

Mary's Gone Crackers, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 6, 2017

iVue with Normative Database, Device Listing Number D185549. Product Usage: The iVue (K121739) is a non-contact, high…

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

Optovue, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 6, 2017

Toshiba America Medical Systems Ultimax Digital Fluoroscopic X-Ray System Model: DREX-UI80 Ultimax is intended for…

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

Toshiba American Medical Systems Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 30, 2017

BUSH'S BEST¿ Brown Sugar Hickory SWEET HICKORY SAUCE WITH BROWN SUGAR & SPICES BAKED BEANS 28 OZ (1 LB 12 OZ) 794 g…

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

Bush Brothers & Co.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 30, 2017

Convertors Robotic Drape with Attached Leggings; Product is packaged as Single Sterile Drape/8 per Case

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

Cardinal Health 200, LLC

FDA (openFDA device enforcement)

Food

Reported Aug 30, 2017

Gold Coast Packing Broccoli Florets; packed in the following configurations: 12 x 2 lb - Product code 508215 - Costco…

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

Fresh Venture Foods, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 30, 2017

DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation (DBS) lead kits, models 3387/3387S, 3389/3389S, and…

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Food

Reported Aug 30, 2017

Medium Coated Jo-Jo Wedges / 00040 (5lb bags)

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

Penobscot McCrum LLC

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 30, 2017

Tissu-Trans Filtron 100, 3-TT-FILTRON 100. Product Usage: Intended for fat transfer and liposuction.

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

Shippert Medical Technologies

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 23, 2017

Arctic Sun 5000 Temperature Management System, 100-120 V North America and 100-120 V US

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 23, 2017

VNS Therapy¿ AspireHC¿ Generator, VNS Therapy¿ AspireSR¿ Generator. Model No. 105. Product Usage: United States…

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

Cyberonics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 16, 2017

BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension, Extension Tube and Latex Straps, 19 oz. Packaged as…

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 16, 2017

iGUIDE Software 2.2 Product Usage: Control of accurate patient positioning with assistance of a 30 Tracking System in a…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 16, 2017

Syringe Bulb, 60 CC 50 pcs per case. The products are used to inject fluids into, or withdraw fluids from the body.…

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

International Medsurg Connection, Inc.

58 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 16, 2017

Sorin Group Aortic Arch Cannula, 7 mm x 10 in x 3/8 in, Rx Only, Sterile Product Usage: The Aortic Arch Cannulae are…

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

Sorin Group USA, Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Aug 12, 2017

Luvo Inc. (USA) Recalls Poultry Products Due To Misbranding and Undeclared Allergens

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

Luvo Inc. (USA)

USDA FSIS

Food

Reported Aug 9, 2017

Professional Formulas Sublinqual B12 High-Potency dietary supplement, 60-count dissolvable tablet in white plastic…

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

Professional Complementary Health Formulas, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 9, 2017

InflammaDry(R) AN RPS DIAGNOSTIC SOLUTION, Sample Collectors InflammaDry(R) is a rapid, immunoassay test for the…

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

Quidel Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 9, 2017

Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid Exchange Catheters Device is indicated for use in…

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

Spectranetics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 9, 2017

ROSA Brain, 3.0.0 The device is intended for the spatial positioning and orientation of instrument holders or tool…

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

Zimmer Biomet, Inc.

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.