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.

Medical devices

Reported Jul 14, 2021

FilmArray Pneumonia Panel (Pneumo) Part Numbers: Part No: RFIT-ASY-0144 / UDI: 00815381020178 (30 test kit) Part No:…

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

BioFire Diagnostics, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 14, 2021

JERSEY COOKIE MONSTER ICE CREAM 3 GALLONS (11.34 LITERS) MFG: GREENWOOD ICE CREAM CO LTD 4829 PEACHTREE ROAD, ATLANTA,…

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

Greenwood Ice Cream

FDA (openFDA food enforcement)

Medical devices

Reported Jul 14, 2021

Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model Number: 20-006-024

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

Luminex Corporation

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 14, 2021

CoreValve Evolut R Delivery Catheter System, REF: ENVEOR-L; ENVEOR-N;

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

Medtronic Heart Valves Division

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 14, 2021

Yakult Nonfat Probiotic Drink; Live and active Lactobacillus casei Shitota; 2.7 FL. OZ. (80 mL), 5 individual bottles…

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

Yakult U.S.A. Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 7, 2021

Edwards TruWave (3 cc)/VAMP Jr 48 in (120 cm) Kit, REF: PXVJ356, Pressure Monitoring Set, RX Only, CE, Sterile EO,…

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

Edwards Lifesciences, LLC

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 7, 2021

PERLA TL Lateral Connector Open - Product Usage: intended to be used with autograft and/or allograft. Pediatric pedicle…

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

Spineart Sa

FDA (openFDA device enforcement)

Medical devices

Reported Jul 7, 2021

Synaptive Trackable Suction Set Standard and Malleable

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

Synaptive Medical Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 7, 2021

Somerdale Red Dragon Cheddar Cheese, cut and repacked in plastic cheese wrap by Wegmans and sold by the pound.

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

Wegmans Food Markets, Inc.

FDA (openFDA food enforcement)

Food

Reported Jun 30, 2021

a.) Banner Smoked Fish Inc. brand Sliced Smoked Scotch Style Salmon (Salmon, Salt, Sugar, Natural Wood Smoke, Sodium…

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

Banner Smoked Fish Inc.

35 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 30, 2021

inLight Medical LED Pads used with Polychromatic light technology system

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

Inlightened Partners LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 30, 2021

reSET Mobile App, iOS and Android, provides cognitive behavioral therapy, as part of substance abuse treatment.

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

Pear Therapeutics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 30, 2021

GENOSYL DS; Nitric Oxide Delivery System Combination Product NDA202860

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

Vero Biotech, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 23, 2021

The Better-Bladder (BB), part of extracorporeal membrane oxygenation (ECMO) cardiopulmonary bypass circuits. Model: BB14

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

Circulatory Technology Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 23, 2021

GE Healthcare Innova IGS 3 (GTIN 00840682147378), Innova IGS 5 (GTIN 00840682124621), Innova IGS 6 (GTIN…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 23, 2021

OSSUR MIAMI J SELECT COLLAR - Product Usage: is intended to provide gross immobilization to the cervical spine. REF:…

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

Ossur Americas

FDA (openFDA device enforcement)

Medical devices

Reported Jun 23, 2021

Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 CPU is also used as spare part.

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

Radiometer Medical ApS

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 16, 2021

Atec Insignia Anterior Cervical Plate System, REF 136-0116, Insignia, ACP, 1-Level, 16 mm, Rx Only, Non-Sterile, UDI:…

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

Alphatec Spine, Inc.

28 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 16, 2021

ExacTrac Dynamic software, Model 20910-01B ETD Positioning and Monitoring Installer 1.0.2 - Product Usage: intended to…

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

Brainlab AG

FDA (openFDA device enforcement)

Medical devices

Reported Jun 16, 2021

DePuy Synthes Articul/eze Femoral Head: Hip joint metal/polymer semi-constrained cemented prosthesis. Part Number:…

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

DePuy Orthopaedics, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 16, 2021

Ruffles All Dressed Potato Chips 16 1/8 oz. packaged in flexible plastic bags UPC 28400 56520

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

Frito-Lay, Inc. Headquarters

FDA (openFDA food enforcement)

Medical devices

Reported Jun 16, 2021

COVID-19 Self-Test Kit *** INNOVA *** 7T

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

Innova Medical Group, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 16, 2021

RayStation (Treatment Planning System) Model Number RayStation is 6.0.0.24 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 ,…

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

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Food

Reported Jun 16, 2021

Mideo's Marinara Glass 32oz jars - 6 jars per case

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

RC Industries Inc.

FDA (openFDA food 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.