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.
Reported Jun 24, 2015
HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and 1103 / OUS: 1100,1101,1102,1104,1104JP and 1205.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2015
CADD¿- Solis Ambulatory Infusion Pump, Model 2111 & 2112, Version 1.0, Version 2.0 and Version 3.0 & Model 2120,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2015
Navigation System II-Cart, 7700-100-000 with Articulated Arm Camera, 7700-103-001 and Articulated Arm Camera,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Jun 24, 2015
T.A.L.O.N (Tactically Advanced Lifesaving Intraosseous Needle) 15G x 38.5 mm 10 NEEDLE SET STERILE EO Single Use Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vidacare Corporation
FDA (openFDA device enforcement)
Reported Jun 17, 2015
AGFA DX-D 100 is a mobile digital radiography x-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Healthcare Corp.
FDA (openFDA device enforcement)
Reported Jun 17, 2015
BBL Port A Cul tubes, catalog number 221606. Patient sample collection tubes. BBL Port A Cul tubes, jars and vials…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2015
Unilateral external fixation ankle clamp Product Usage: Unilateral external fixation for use treatment of bone…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2015
Roscoe Mini Neb Compressor User Manual for the NEB-ROS Product Usage: Inhaler therapy that converts liquid medicine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Compass Health Brands
FDA (openFDA device enforcement)
Reported Jun 17, 2015
Ally Uterine Positioning System (Ally UPS) used in the mounting and positioning and holding of uterine manipulators…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Jun 17, 2015
GE OEC Brivo 865 plus, Mobile X-ray system laser aimer assemblies (part number 520002DW)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jun 17, 2015
Golden Krust SOYA PATTIES, NET WT. 17.2 LBS, 50 UNBAKED, KEEP FROZEN
High riskUsing this product could cause serious injury, illness or death — stop using it now.Golden Krust Caribbean Bakery, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 17, 2015
HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and 1103 / OUS: 1100, 1101,1102,1104,1104JP and 1205.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2015
Rugby Poly Vitamin Liquid, 50ml
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pharmatech LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 17, 2015
M/L Taper with Kinectiv¿ Technology. prosthesis, hip, semi-constrained (metal uncemented acetabular component) Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Jun 10, 2015
Oncentra Brachy radiation therapy planning software designed to analyze and plan radiation treatments in three…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2015
Alere i Influenza A & B Product Usage: The Alere i Influenza A and B assay, performed on the Alere i Instrument, is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere Scarborough, Inc. dba Binax, Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2015
D2-40 (Lymphatic Marker); For In Vitro Diagnostic; Catalog number: PM266AA Product Usage: In Vitro Diagnostic Use.: a…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Biocare Medical, LLC
FDA (openFDA device enforcement)
Reported Jun 3, 2015
KimVent Turbo-Cleaning Closed Suction System for Adults, 10 F T-Piece (Product Code 227105); KimVent Turbo-Cleaning…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Halyard Health, Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2015
100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for…
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)
Reported May 27, 2015
ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip, Product Usage: The instruments have application in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported May 27, 2015
Jose' Madrid SALSA BLACK BEAN CORN POBLANO SALSA NET WT 13 OZ (369 G) www.josemadridsalsa.com Jose Madrid Salsa PO Box…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Michael Zakany LLC
FDA (openFDA food enforcement)
Reported May 27, 2015
Mucolytic Agent 1 pint/473 ml; 1 gallon/3.8 l Product Usage: A mucoliquefying preservative designed for use in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richard-Allan Scientific Company
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 27, 2015
Homocysteine test system - Homocysteine Reagent. 05385415190; Homocysteine 100 Tests, cobas c, COBAS INTEGRA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported May 27, 2015
The product comes in a 4-ounce clear plastic tear-strip enclosed container. The pine nuts are sold in store Produce…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Superior Nut & Candy Dist. Co.
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.