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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.

Medical devices

Reported Aug 22, 2018

Rio System Irrigation Clip - Catalog # 111690 Product Usage: The RESTORIS Partial Knee Application (PKA) for use with…

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

Mako Surgical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 22, 2018

1mL Medallion Syringes 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.

Merit Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 22, 2018

CDI Blood parameter monitoring system 500 H/SAT, Part No. 145883 Product Usage: The CDI System 500 provides continuous,…

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

Terumo Cardiovascular Systems Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 15, 2018

AnnaSea Wasabi Ahi Poke Hawaiian Poke Kits

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

Aldi Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 15, 2018

Boston Scientific Guider Softip XF Guide Catheter Product Usage: Is a neurovascular access catheter that creates a…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Food

Reported Aug 15, 2018

Swiss Rolls***Brand Name**Swiss Rolls Chocolate (Snack) Cakes, NET WT OZ (g) PKGS***TWIN PACKS***Nutrition…

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

Flowers Foods

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 15, 2018

119" Blood Set w/200 Micron Filter, Clave¿, Rotating Luer, Sterile The blood tubing accessory with CLAVE Connector is a…

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

ICU Medical, Inc.

52 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 15, 2018

Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Export For PTZ Video Ext, IP PTZ HD ErgoJust Video…

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

Natus Neurology dba Excel Tech., Ltd. (XLTEK)

FDA (openFDA device enforcement)

Food

Reported Aug 15, 2018

Ocean Delight Individually Vacuum Packed AHI TUNA SAKU, 8-12 oz. NET WT. 10 LB (4.54 kg) and 12-16 oz. NET WT. 22LB…

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

Stavis Seafoods, Inc.

FDA (openFDA food enforcement)

Food

Reported Aug 15, 2018

Pictsweet Farms Steam'ables Baby Brussels Sprouts***NET WT 12 OZ (340g)***THIS SIDE UP IN MICROWAVE***Nutrition…

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

The Pictsweet Company

FDA (openFDA food enforcement)

Food

Reported Aug 15, 2018

utz Carolina Style Barbeque Potato Chips, Net Wt 2.875 OZ, UTZ Quality Foods, LLV, Hanover, PA 17301, UPC:…

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

Utz Quality Food Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 15, 2018

AirLife Resuscitation Device, Adult labeled as the following: a. Adult, with mask, oxygen reservoir bag, Part Number…

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

Vyaire Medical

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 15, 2018

Waterpik Sonic-Fusion Professional, Model: SF-02 Product Usage: The device is composed of a unit base and an oral…

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

Water Pik, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

VIDAS LH, Reference Numbers 30406 and 30406-01. Poduct Usage: VIDAS LH is an automated quantitative test for use on the…

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

bioMerieux, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

Drill (Fluted-Hard Bone), for Quattro Link 2.9mm, labeled as: a. Quattro Spade Drill, for 2.9mm, Model Number CM-9300;…

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

Cayenne Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

1) ELITE HV, Hemostasis Valve Introducer System, Sterile EO, Rx Only, Catalog #: a) BCL-100-04; b) BCL-100-05; c)…

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

Galt Medical Corporation

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

Discovery IQ 2.0 20cm, 4 ring, Model Number 5432539-22

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

GE Healthcare, LLC

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

MAYFIELD INFINITY XR2 BASE UNIT, Part Number A2079 The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to…

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

Integra LifeSciences Corp.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

VNS Therapy Programming System, Rx Only, Model 3000, v1.0.2.2

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

XLTEK EMU40EX EEG Headbox

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

Natus Neurology dba Excel Tech., Ltd. (XLTEK)

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

Nicolet¿ Ambulatory EEG

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

Natus Neurology Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 8, 2018

Food Lion Dill Pickle Flavored Potato Chips 7.75 oz. package bag/12 bags per case

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

Shearer's Snacks

FDA (openFDA food enforcement)

Medical devices

Reported Aug 1, 2018

Arctic Sun Temperature Management System, Model 5000. The Arctic Sun¿ 5000 model is a non-invasive, thermal regulating…

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

Bard Medical Division

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

PR4100 Microplate Reader US, Catalog Number 45591587 Product Usage: The PR4100 Microplate Reader is a 96 well…

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

Bio-Rad Laboratories 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.