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 48,124 notices were distributed nationwide, so they reach North Carolina too — those are in the archive.
Reported Dec 17, 2014
ESSENTIA Hydration Perfected Purified Water and Electrolytes, 9.5 pH, Manufactured for Essentia Water Inc., 22833…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nature's Way Purewater Systems, Inc.
FDA (openFDA food enforcement)
Reported Dec 17, 2014
Covidien Puritan Bennett 980 Ventilator, Rx ONLY, Made in Ireland., Covidien LLC, USA. REF 980X1ENDIUU.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nellcor Puritan Bennett Inc. (dba Covidien LP)
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Rapid Centesis Catheter, 5 Fr x 7 cm Catheter, Ref No. M7513 Product Usage: Short term percutaneous fluid drainage
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pfm Medical Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 17, 2014
BrightView XCT is a gamma camera for Single Photon Emission Computed Tomography (SPECT) and integrates with an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Align Radial Stems, Prosthesis, Elbow, Hemi Replacement of the radial head for degenerative or post-traumatic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Skeletal Dynamics
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Crocodile (size 3) are two-armed, wheeled walking aids, used by children with disabilities. Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Snug Seat Inc.
FDA (openFDA device enforcement)
Reported Dec 17, 2014
TomoTherapy Treatment System with software versions 2.0.1 / 2.0.2 / 2.0.3/ (Hi:Art 5.0.1 / 5.0.2 / 5.0.3)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TomoTherapy Incorporated
FDA (openFDA device enforcement)
Reported Dec 10, 2014
Amerigel Hydrogel Wound Dressing Wound management
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerx Health Care Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 10, 2014
MAS CardioImmune XL Cardiac Marker Control; Model: CAI-XL1; intended for use in the clinical laboratory as an assayed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microgenics Corporation
FDA (openFDA device enforcement)
Reported Dec 10, 2014
Queso Seco Centroamericano (Cheese) in individually soft poly/plastic bags labeled in part: Lacteos Santa Martha Queso…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oasis Brands, Inc.
15 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 10, 2014
Gourmet Warehouse, Red Wine Marinade, 16 fl.oz. (473 mL), Ingredient: Soy Sauce, Salt, Black Pepper, Cayenne Pepper,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.R and S Gourmet Warehouse
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 10, 2014
Aquapak Adaptor, 028 NEB, INTL, Product No. 403128; Aquapak Adaptor, 033 NEB, INTL, Product No. 403133; Aqaupak…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2014
ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 or 4 Bottle(s) (6.6 mL/27.0 mL) anti-T3 (sheep) coated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
FDA (openFDA device enforcement)
Reported Dec 3, 2014
Abbott m2000sp, an automated system for performing sample preparation for nucleic acid testing.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Molecular
FDA (openFDA device enforcement)
Reported Dec 3, 2014
Los Chileros de nuevo mexico gourmet southwestern cuisine Blue Corn Waffle & Pancake Mix, Net Wt. 16 oz (453.6 grams),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Los Chileros De Nuevo Mexico, Ltd.
6 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 3, 2014
LUNA Chest, Model No. LU4006
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Novadaq Technologies, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2014
Remel TB Potassium Permanganate (.5% Aqueous) 40192, packaged in 250 ml bottles, 5/pkg. A stain for use in qualitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2014
Trabecular Metal Tibial Impactor. Product Usage: TM Tibial Impactor pads are used in conjunction with the TM Tibial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2014
7F NeuroFlo Catheter, Model 1027 The NeuroFlo Catheter is a multi-lumen device with two balloons mounted near the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZOLL Circulation, Inc.
FDA (openFDA device enforcement)
Reported Nov 26, 2014
CyberKnife Robotic Radiosurgery System with the first generation IRIS Variable Aperture Collimator. The CyberKnife is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accuray Incorporated
FDA (openFDA device enforcement)
Reported Nov 26, 2014
Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Biomerieux
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 26, 2014
GOLDEN LION brand DRIED ZIZIPHUS JUJUBA MILL (DRIED DATES), NET WT. 12 oz (340 g), UPC 7 34765 04008 6 -- PRODUCT OF…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Blooming Import Inc.
FDA (openFDA food enforcement)
Reported Nov 26, 2014
Edwards Lifesciences Vent Catheters, . Packaged sterile and non-pyrogenic in a sealed, peel-type pouch. Model Numbers:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Nov 26, 2014
SideFire Directional Laser Probe, REF: NBP101-01, NBP201-01, NBP301-01, NBP401-01, NBP501-01. These laser probes are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Monteris Medical Corp.
1 more product in this recall
FDA (openFDA device 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.