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 Feb 11, 2015
MobileDiagnost wDR motorized portable diagnostic X-ray systems.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sedecal S.A.
FDA (openFDA device enforcement)
Reported Feb 11, 2015
16cm Minimally Invasive Attachment. For use with Motor Systems for cutting and shaping bones, including the spine and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported Feb 4, 2015
Airo Mobile Intraoperative CT I Airo; Model #: MobiCT-32. Computed Tomography x-ray system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mobius Imaging, LLC
FDA (openFDA device enforcement)
Reported Feb 4, 2015
Bologna & Cheese, Net Wt. 3.00 oz., UPC 7-01248-00309-9, MFG Code 1038; Thick Bologna & Cheese, Net Wt. 4.50 oz., UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.SunBurst Foods, Inc.
120 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 4, 2015
Thera Tablets with Beta Carotene Dietary Supplement
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The Harvard Drug Group, LLC
FDA (openFDA food enforcement)
Reported Feb 4, 2015
Market Pantry Brand Dark Chocolate Covered Almonds 9 oz., UPC 085239555644
High riskUsing this product could cause serious injury, illness or death — stop using it now.Zachary Confections, Inc.
FDA (openFDA food enforcement)
Reported Jan 28, 2015
FLUTTER Percussor respiratory device, packaged one unit per clear plastic package. Product Usage: Product is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aptalis Pharmatech Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2015
Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Jan 28, 2015
PF4 Concentrated Wash (10x), REF 403624, packaged in the following assay kits: 1. ImmucorGamma LIFECODES PF4 IgG…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Genetic Testing Institute,Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2015
VITROS Software Version 3.1 utilized on the following systems: 1) 4600 Chemistry Systems (VITROS 5,1 FS System family…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Jan 28, 2015
Philips IntelliVue TcG10; Monitor, carbon-dioxide, cutaneous. The IntelliVue TcG10 is a device for the measurement of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2015
QuestBar Protein Bar Double Chocolate Chunk Flavor NET Wt. 2.12 OZ (60g) Lot #: 1BA4DCC14289 Exp Date: October 17, 2015…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quest Nutrition, LLC.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 21, 2015
The Abbott m2000sp is 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 Jan 21, 2015
iPlan RT Dose is a stereotactic radiation treatment planning system that is intended for use in stereotactic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Philips Expression MR200 MRI Patient Monitoring System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Jan 21, 2015
POWEREASE Instruments Set Screw Breakoff Instrument, REF 2346010, Medtronic Sofamor Danek, USA, Inc. Spinal surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Sofamor Danek USA Inc.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
MENTOR MemoryGel Resterilizable Gel Sizer Moderate Plus Profile STERILE. Breast prosthesis sizer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mentor Texas, LP.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Phadia 1000 Instrument (introduced as UniCAP 1000), Article number: 12-3800-01 (All instrument software versions since…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phadia US Inc.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Various Brilliance and Ingenuity Computed Tomography X-ray systems; one unit per package Product Usage: Intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Drill set long, drill stop compatible for 4.8mm diameter implant, Article Number 040.447S Endosseous dental implant…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straumann USA, LLC
FDA (openFDA device enforcement)
Reported Jan 21, 2015
The SurgiCounter Charging Cradle Product Usage: SurgiCounter Charging Cradles are designed to be used with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform ophthalmic surgeries.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ziemer USA Inc.
FDA (openFDA device enforcement)
Reported Jan 14, 2015
Baxter Amia Automated PD systems are used in the treatment of adult renal failure patients to perform automated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 14, 2015
CSA Medical truFreeze System; Model: CC3-01, a cryogenic surgical device ***The involved units are those with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CSA Medical
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new North Carolina recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.