All recall categories

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 48,100 notices were distributed nationwide, so they reach Nevada too — those are in the archive.

Medical devices

Reported Jan 25, 2017

PREMIER EHEC and PREMIER EHEC Bulk.

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

Meridian Bioscience Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 18, 2017

In The Mix¿ Monkey Bread Mix NET WT 16 oz (16 lb) 454 g box, INGREDIENTS: BREAD MIX: ***BUTTERMILK*** DISTRIBUTED BY…

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

Brand Castle LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jan 18, 2017

SURESTEP Tray, BARDEX I.C. COMPLETE CARE, Urine Meter, Temperature STATLOCK Stabilization Device

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2017

OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the…

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

GE OEC Medical Systems, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2017

Merge Eye Station f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager…

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

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2017

Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT, CR3434CT Ablation catheter cables are designed as…

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

Stryker Sustainability Solutions

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 11, 2017

GalaSHAPE 3D; product code SH3D03, a medium size oval GalaSHAPE" 3D is indicated for use as a bioresorbable scaffold…

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

Tepha Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Jan 4, 2017

Innova 2000

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

GE Healthcare, LLC

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 4, 2017

Specimen Gate Laboratory 5002-0180, Specimen Gate eReports 5002-0370, Software Version 1.0 Specimen Gate Laboratory is…

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

PerkinElmer Health Sciences, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 4, 2017

Shimadzu X-ray TV System, Catalog No. SONIALVISION G4

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

Shimadzu Medical Systems

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 4, 2017

Bionix, 30 capsules per bottle

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

Sunset Natural Products Inc.

162 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 4, 2017

Limu Poke is fresh refrigerated product, distributed in bulk kit, net wt. 4.35 lbs. Each kit includes five individually…

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

Western United Fish Company, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 28, 2016

BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath¿…

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 28, 2016

Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit

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

Exactech, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 28, 2016

Affinity Fusion" Oxygenator with Integrated Arterial Filter, Affinity Fusion cardiotomy/Venous Reservoir, Perfusion…

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

Medtronic Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 28, 2016

Merge OrthoCase software. The firm name on the label is Merge Healthcare, Hartland, WI.

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

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 28, 2016

White Fudge Oreo, brand Real Fudge. Product is sold in clear plastic deli container in 8 oz. and 16 oz.

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

Real Fudge

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 28, 2016

Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit including the Ultroid Disposable Sterile Probes

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

Ultroid Technologies, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 21, 2016

Back to Nature, Gluten-Free, Chocolate Delight Granola, 11 oz.(311g) pouches, 6 per case. UPC 8-19898-01201-5.

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

Back To Nature Foods, LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 21, 2016

Cook Spectrum Minocycline/Rifampin Impregnated Double Lumen Central Venous Catheter Tray Cook Spectrum…

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

Cook Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 21, 2016

Pesto Pasta Salad with Arugula, Net Wt. 16oz, UPC 857898004333

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

Green Cuisine, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 21, 2016

INOVO Purefill Oxygen Compressor Model PF1100 Is an oxygen refill machine that you can attach to an oxygen concentrator…

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

Inovo, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 21, 2016

Roasted & Salted Sunflower Kernels under the following brand names: AMISH FARMS SALEM, OHIO 44460 5.5 oz plastic bag…

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

Ohio Hickory Harvest Brand Products Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 21, 2016

Trader Joe's Mediterranean Hummus SKU #90642

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

Two Chefs On A Roll, Inc.

1 more product in this recall

FDA (openFDA food 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.