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 48,132 notices were distributed nationwide, so they reach North Carolina too — those are in the archive.
Reported Apr 3, 2013
BS-200 Chemistry Analyzer Designed for clinical laboratory use.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. d.b.a. Mindray North America
FDA (openFDA device enforcement)
Reported Apr 3, 2013
Intraosseous Fixation System (IFS) 1.7 mm, 2.0 mm & 2.5 mm Cannulated Drill Bit. Intended to stabilize and aid in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthohelix Surgical Designs Inc.
FDA (openFDA device enforcement)
Reported Apr 3, 2013
PHYSICIANS TOTAL CARE, TETRACYCLINE, 250 mg, 30 CAPSULES, bottle MFG. BY: TEVA PHARMACEUTICALS USA, SELLERSVILLE PA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physicians Total Care, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Apr 3, 2013
Siemens Dimension Vista(R) Alkaline Phosphatase (ALP) Calibrator The ALP CAL is an in vitro diagnostic product for the…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Apr 3, 2013
Siemens Axiom Artis zeego systems with software version VC14, VC20 and VC21 in conjunction with specific technical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 3, 2013
Synthes Dens Instrument Set (Dens Graphic Case), Part Number 687.030 (also known as the Anterior Column Retractor Set)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes USA HQ, Inc.
FDA (openFDA device enforcement)
Reported Mar 27, 2013
ILLICO Straight CP TI Rod, -5.5MM x 110M; REF#73601-110; Qty 1; LBL-005; REV.B; RX ONLY; Alphatec Spine, Inc. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alphatec Spine, Inc.
FDA (openFDA device enforcement)
Reported Mar 27, 2013
Boston Scientific/Cameron Health SQ-RX Model 1010 subcutaneous pulse generators. The S-ICD System is intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific CRM Corp.
FDA (openFDA device enforcement)
Reported Mar 27, 2013
Spacelabs BleaseSirius Anesthesia Workstation, BleaseFocus Anesthesia Workstation, and CAS I/II Absorber contained in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Del Mar Reynolds Medical, Ltd.
FDA (openFDA device enforcement)
Reported Mar 27, 2013
Optetrak Logic Comprehensive Knee Prosthesis System, Proximal Tibial Spacer and screws, size 3.5, 8mm, Catalog #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Mar 27, 2013
Extremity Medical - Disposable Orthopedic Surgical Instrument - 1.6 mm Guidewire - Reference Number 101-00006 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Extremity Medical LLC
FDA (openFDA device enforcement)
Reported Mar 27, 2013
Siemens Dimension(R) Tacrolimus Flex(R) reagent cartridge (DF107). The TACR method is used as an in vitro diagnostic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Mar 27, 2013
Dannon Activia LIGHT Nonfat Yogurt Peach Flavor 4x4oz cups INGREDIENTS: CULTURED GRADE A NONFAT MILK, WATER, PEACHES…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Dannon Company, Inc. - Discovery & Innovation Center
2 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 27, 2013
Vascular Solutions, Inc., Guardian II and Guardian II NC Hemostasis Valve, used in cardiopulmonary bypass. Model…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Mar 20, 2013
55613210946 Western Family, Easy Sides, Herb & Butter Pene, Net WT 5.5 oz (156 g), UPC "0 15400 12655 7", Proudly…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bay Valley Foods LLC/ TreeHouse Foods, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 20, 2013
Elekta Synergy XVI. Radiation Therapy Digital Imager. Product XVI R3.5.1, R4.2.1, and R4.5.1 Used as part of radiation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Mar 20, 2013
GE Healthcare, Innova 2100 IQ, Innova 3100 IQ, Innova 4100 IQ. Cardiovascular X-ray imaging systems. For use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 20, 2013
ANTI-BORRELIA (LYME) MICROPLATE EIA Kit, Catalog # 32507 Kit Lot Number 120960. Package Insert Supplement:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Innominata dba Genbio
FDA (openFDA device enforcement)
Reported Mar 20, 2013
Genesis Straight Esthetic 4.0 mm 1mm Cuff Abutment Part Number: G71200 Genesis implant for single stage or two stage…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keystone Dental Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 20, 2013
Brilliance 6, 10, 16, 40, 64, Big Bore and the iCT, iCT SP, Ingenuity CT and MX8000 Dual v. EXP are Computed Tomography…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 20, 2013
INTERNAL HEX RECON SCREW, TI-6AL-4V, REF 7162380, TRIGEN (R) INTERNAL HEX CAPTURED RECON SCREW, QTY: (1), 6.4 MM, 80…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 20, 2013
GOPump Elastometric infusion PumpKit with/ and without accesssories all containing Dual GOPump, part number 510076: One…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Symbios Medical Products, LLC
FDA (openFDA device enforcement)
Reported Mar 20, 2013
365 Organic Orzo, 16oz, 20 carton/case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Whole Foods Market
2 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 13, 2013
Deep Best Quality Dry Garlic Chutney (Thechaa); Net Wt. 4 OZ.; UPC 011433111201; Deep Foods, Inc. Union, NJ 07083
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Deep Foods 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.