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Recalls distributed in Nevada

These notices name Nevada 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.

2,512 stored notices name Nevada, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Nevada too — those are in the archive.

Medical devices

Reported Aug 21, 2013

ADVIA Centaur Calibrator A. Cat. #04800735, SMN 10285904 (6 pack); Cat. # 04800840, SMN 10285905 (6 pack - REF). For…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2013

Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***REF Cat. No.***466F220A and 466F220B***Vena Cava Filter and…

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

Cordis Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2013

Medtronic Mullins Transseptal Adult 7F, REF 008551. Intended for the introduction of cardiovascular catheters into the…

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

Medtronic Inc. Cardiac Rhythm Disease Management

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2013

Nestle Nutrition, Compat, Enteral Feeding Tube, sterile, 8 French (REF 08310400), 10 French (REF 08310600), and 12…

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

Nestle HealthCare Nutrition

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2013

TCM4 series Base Units, and spare part Power Supply, Radiometer Medical ApS, Akandevej 21, Br¿nsh¿j, Denmark,…

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

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2013

Sonopet Ultrasonic Aspirator Console (Console 110V with Pedal & Pole) Product Usage: The Sonopet Console is indicated…

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 Aug 14, 2013

Raw Pistachio Halves, 1 pound bag. Item Number 11910, UPC Code: 172043119107; Raw Pistachio Halves, 4 pound bag. Item…

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

Superior Nut Co. Inc.

FDA (openFDA food enforcement)

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)

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

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 Jul 31, 2013

ProSpace Peek Implant 5 degree x 8.5 x 22 mm The device is intended for vertebral body replacement or intervertebral…

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

Aesculap, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 31, 2013

601009 ANTIOXIDANT SUPERSTAR MIX 100/2 OZ FLAT PACK, UPC 2052601009 601076 ANTIOXIDANT SUPERSTAR MIX 12/6 OZ BERGIN RED…

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

Bergin Fruit And Nut Co. Inc.

9 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)

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)

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

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)

Medical devices

Reported Jul 17, 2013

Integra Hallu-Fix cannulated screw driver (model number P/N 129733ND) and cannulated screwdriver tip (model number P/N…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Food

Reported Jul 17, 2013

R.L. Schreiber Batter Mix, 2.5 lb packaged in white flexible plastic bag, 12 bags per case.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

R.l. Schreiber Inc. - Lebanon

FDA (openFDA food enforcement)

Food

Reported Jul 17, 2013

"***JENSEN'S SEATTLE STYLE SMOKED WILD PACIFIC SALMON ***JENSEN'S SMOKEHOUSE, INC.***10520 GREENWOOD AVE N***SEATTLE,…

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

Salmolux (A Pacific Seafood Group Company)

5 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 17, 2013

Treasured Harvest-Roasted & Salted Pistachios, 5lbs, 12oz, 6oz

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

Western Mixers Produce & Nuts, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 10, 2013

Fudge Buttercream Frosted Peanut Butter cookies, some of which were mislabeled by being wrapped in Buttercream Frosted…

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

Cheryls

FDA (openFDA food enforcement)

Medical devices

Reported Jul 10, 2013

GE Healthcare, Innova 3100 and Innova 4100 systems. The Digital Fluoroscopic Imaging System is indicated for use in…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

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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.