All recall categories

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 48,868 notices were distributed nationwide, so they reach North Carolina too — those are in the archive.

Medical devices

Reported Aug 7, 2013

LPS Lower Extremity Dovetail Intercalary component. Intended for use in replacement of the mid-shaft portion of the…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

DePuy Orthopaedics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 7, 2013

GE Healthcare, VOLUSON E6, E8, E8 EXPERT, E10 DIAGNOSTIC ULTRASOUND SYSTEM. The device is a general purpose ultrasound…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 7, 2013

Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

HeartWare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 7, 2013

The Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, drugs, agents, nutritionals,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hospira Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 7, 2013

OSKRI, Coconut Bar Dark Chocolate, Net Wt. 1.9 oz ( 53g), UPC 6 66016 30070 3. Ingredients: Coconuts 55%, Rice Syrup,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Oskri Corp.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 7, 2013

Synthes Large External Fixation, MR Conditional, Tube to Tube Clamp, Part Number 390.007, Lot Number 6800599 Synthes…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Synthes USA HQ, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 7, 2013

AIA Analyzer Pipette Tips used on Tosoh AIA-2000, AIA-1800, AIA-900 and AIA-600II Analyzers, 1000 tips/bag AIA-Analyzer…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tosoh Smd Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 7, 2013

uTASWako DCP, Lot TG340 2013.11, REF 995-60701, Wako Pure Chemical Industries, Ltd. 1-2 Doshomachi 3-chome, Chuo-Ku…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Wako Life Sciences, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 31, 2013

Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a licensed Chiropractor to assist in making…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Advanced Orthogonal Equipment, Incorporated

FDA (openFDA device enforcement)

Food

Reported Jul 31, 2013

Vanilla almond granola, Net WT 16 oz(454g), UPC 0 71725 71239 4, Distributed by American Importing Co., Inc,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

American Importing Co., Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 31, 2013

Endopath Electrosurgery Probe Plus II, twelve (12) different devices, including hooks, spatulas, right angles, curved…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ethicon Endo-Surgery Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 31, 2013

Master Cases, Product Code #8534 (6-12 count retail boxes) Label of master case bears the name: Donut House K -Cup…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Green Mountain Coffee Roasters

FDA (openFDA food enforcement)

Medical devices

Reported Jul 31, 2013

HemosIL RecombiPlasTin 2G, Part Number 0020002950 (8 ml size). The product is used for the evaluation of the extrinsic…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Instrumentation Laboratory Co.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 31, 2013

Rultract Retractor Ratchet Cover Plate Distributed by Pemco, Inc., Cleveland, OH 44131 Surgical retractor used to lift…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Pemco Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 31, 2013

The LIFEPAK 500 Automated External Defibrillator is a semi-automatic defibrillator that uses a patented Shock Advisory…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Physio Control, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2013

MedStream Programmable Infusion Pump- Implantable for the intrathecal delivery of Baclofen or Morphine Product…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Codman & Shurtleff, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 24, 2013

PISTACHIOS-INSHELL-R/S-21/25-6.25LB, Net Wt. 6.25 LB. Item number: 920. Product is packed in a clear plastic liner then…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Nassau Candy

FDA (openFDA food enforcement)

Medical devices

Reported Jul 24, 2013

B-CrossLaps/serum (B-CTx in serum) REF 11972308 160 100 tests Immunoassay for the in vitro quantitative determination…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2013

Siemens AXIOM Artis zee/zeego systems equipped with generator A100 Plus Product Usage: Angiographic x-ray system

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 24, 2013

Somersault Pacific Sea Salt flavor, crunchy nuggets baked with sunflower seeds and toasted grains. 1 oz. packages sold…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Somersault Snack Co., LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jul 24, 2013

nanoFLEX CC4204A Intraocular Lens Correct aphakia in persons 60 years of age or older in whom a cataractous lens has…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Staar Surgical Co.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2013

Stryker TPS Universal Driver REF 5100- 99 Rx , The Stryker Total Performance System (TPS) is intended for use in the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Instruments Div.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 24, 2013

Talenti Gelato, Toasted Almond, One Pint (473ml), Crafted by: Talenti, Marietta, GA 30062

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Talenti Gelato

FDA (openFDA food enforcement)

Medical devices

Reported Jul 24, 2013

CDI Blood Parameter Monitoring System 500 with Arterial and Venous blood parameter modules and Hematocrit/Saturation…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Terumo Cardiovascular Systems Corporation

4 more products 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.