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.
4,767 stored notices name North Carolina, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,853 notices were distributed nationwide, so they reach North Carolina too — those are in the archive.
Reported Sep 7, 2016
Euro Custard Cake, Plastic wrapped cardboard container (Net Wt. 7.20 oz.)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Eastland Food Corporation
FDA (openFDA food enforcement)
Reported Sep 7, 2016
FUJIFILM Digital Mammography System Aspire HD (FDR MS-1000) with Biopsy Positioner (FDR-1000BPY) The Fujifilm Digital…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fujifilm Medical Systems U.S.A., Inc.
FDA (openFDA device enforcement)
Reported Sep 7, 2016
Chili Dog, Low Fat/Low Sodium Product ID 952000
High riskUsing this product could cause serious injury, illness or death — stop using it now.Let's Do Lunch, Inc.
8 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 7, 2016
Double Pump RF Patient Cassette; Product Number: 72204055. Intended to provide fluid distension and irrigation and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Vision Ab
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.), 10' (3.05m) Cable, Catalog Number 51-7310.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Conmed Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
CARESCAPE VC150 Vital Signs Monitor; Intended to monitor a single patient's vital signs at the site of care.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Innokas Medical Oy
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Large QWIX Compression screw, dia. 7.5 mm L 90 mm, Lot No. FH86, Rx only, Product Usage: The QWIX Positioning screw is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Medtronic, Viva Quadripolar Implantable Cardioverter Defibrillators: Product Model VIVAXTCRT-D DTBA1D1, DTBA1D4…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
RadSuite software. The firm name on the label is Merge Healthcare, Hartland, WI.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Radiesse (+) Lidocaine, Injectable Implant 1.5cc, Rx only, P/N: 8063M0K1, Merz Aesthetics. Product Usage: RADIESSE is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merz North America, Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
The Cheese & Berries Danish was labeled Pleasant Hill Ovens, Cheese Danish, Artificial Flavored, Net WT 5.0 OZ (142 g),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Northern Tier Bakery (dba\ Super Mom's)
FDA (openFDA food enforcement)
Reported Aug 31, 2016
TIGR Matrix Surgical Mesh, Model No. NSTM1015, NSTM1520, NSTM2030
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novus Scientific Ab
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Brilliance 64 CT Model number 728231 Product Usage: Computed Tomography X-ray systems intended to produce…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Conical portio adapter (acorn) small & large are used for examination and diagnosis in conjunction with endoscopic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richard Wolf Medical Instruments Corp.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Infinite F50 instrument. The INFINITE F50 instrument is a 96-well absorbance reader for the measurement of light…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tecan US, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 24, 2016
Xpert MRSA Catalog GXMRSA-120, Rev. AJ Microbiology: The Cepheid Xpert MRSA assay performed in the GeneXpert Dx System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cepheid
FDA (openFDA device enforcement)
Reported Aug 24, 2016
Hospira RECEPTAL CANISTERS: 1L(1000mL), 1.5L(1500mL), 2L(2000mL) Canister, ATS, 2000, with Valve 1) List Numbers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 24, 2016
Weck EFx Classic Fascial Closure System, Rx Only, Sterile, The product is intended to facilitate placement and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Aug 17, 2016
BD Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD); Catalog number 340383. Label states: Contains CD3 FITC/CD4 PE/CD45 per CP…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported Aug 17, 2016
NucliSENS easyMAG Magnetic Silica The NucliSENS easyMAG accessory products are reagents and disposable to be used with…
High riskUsing this product could cause serious injury, illness or death — stop using it now.BioMerieux SA
FDA (openFDA device enforcement)
Reported Aug 17, 2016
Coolife Sinergy Radiofrequency Kit, SIK-17-75-4 (109971504); Kit used in conjunction with a Radiofrequency Generator to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Halyard Health, Inc.
FDA (openFDA device enforcement)
Reported Aug 17, 2016
Hitachi Scenaria Computed Tomography System Hitachi Medical Systems America, Twinsburg, OH 44087
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Aug 17, 2016
lnvacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16. Packed one per carton. The lnvacare Precise Rx Pediatric…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 17, 2016
Sundae Shoppe Novelty Ice Cream Dipped "Variety"cones, 32 oz. box, Manufactured by Mister Cookie Face LLC, Lakeland, NJ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mister Cookie Face Corporation
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.