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.

4,753 stored notices name North Carolina, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach North Carolina too — those are in the archive.

Medical devices

Reported Mar 18, 2026

HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product Number: VSLBASE03P / VITALSYNCSW03…

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

Covidien LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2026

Artelon FlexBand Dynamic Matrix Ref: 31057

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

International Life Sciences

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 18, 2026

VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ingredients: Enriched unbleached flour (wheat flour***)…

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

Palmetto Gourmet Foods Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 18, 2026

PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code:…

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2026

Raz-AT (Attendant Tilt) Mobile Shower Commode Chair, Catalog Number Z300 UDI-DI code: (01)00628758003007 Raz-ART…

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

Raz Design Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 18, 2026

Lowes Foods sour cream and onion flavored potato chips, 8oz. bag, UPC 7 41643 05576 6, 9 retail units per case

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

Uncle Ray's LLC

FDA (openFDA food enforcement)

Medical devices

Reported Mar 11, 2026

Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software…

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

Aesculap Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2026

Brand Name: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S Model/Catalog Number (REF): 00516…

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

Diagnostica Stago, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2026

Esaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038

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

Esaote S.p.a.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2026

Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE, 633010PE, 633007PE, 636010PE, 632522PE, 633012PE, 635018PE,…

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

Vascutek, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2026

PIE Trolley System Model: 2005

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

Edermy LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2026

MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery is used in conjunction with…

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

MRIMed Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 4, 2026

NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) INGREDIENTS: CERTIFIED ORGANIC CHIA SEED (SALVIA HISPANICA).…

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

Navitas, LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 25, 2026

MONARCH Platform, Bronchoscopy, Catalog Numbers: MON-000005-01 , MON-000005-01R , MON-000006 , MON-000006-RFB,…

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

Auris Health, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 25, 2026

Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 25, 2026

Estrone RIA, REF: DSL8700

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

Immunotech A.S.

FDA (openFDA device enforcement)

Food

Reported Feb 25, 2026

Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset, Net Wt., 1 fl oz (30 ml) liquid…

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

Pure Solutions, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 25, 2026

MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marker UDI (GTIN):…

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

Stryker Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 25, 2026

Teslatome Bipolar Sphincterotomes REF: TESLA-B2535-260 Model Number: G60784 UDI-DI code: 00827002607842 REF:…

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

Wilson-Cook Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 18, 2026

ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 266-01-000-10-N UDI-DI code: 00190376476179;…

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

Alphatec Spine, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 18, 2026

Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11.1 Product…

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

Elekta, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 18, 2026

da Vinci 5 Surgeon Console Viewer Display, ASSY, DV5 CONSOLE, IS5000, Part Number: 380730-45

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 18, 2026

Brilliance iCT; Product Code (REF): 728306;

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

Philips North America LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 18, 2026

Barco MNA with the HexaVue IP Integration System, Model/Catalog Number: MNA-6x0-H

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

Steris 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.