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.
Reported Mar 15, 2017
A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni Part No. 324124. Prism Medical.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ErgoSafe Products, LLC (DBA) Prism Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 15, 2017
Great Shake Fortified Nutrition, Soy Formula, Chocolate Artificially Flavored, Packaged in 4 fl oz. (118 mL), and 6 fl…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hormel Foods Corporation
5 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 15, 2017
RBR Meat Company, Inc. Recalls Frozen Pizza Product Due to Possible Listeria Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.RBR Meat Co., Inc.
USDA FSIS
Reported Mar 15, 2017
Color contact lenses labeled under the following brands: Diamond, Fierce, Ambition, Circle Collection, Lunatic, Fright,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The See Clear Company
FDA (openFDA device enforcement)
Reported Mar 15, 2017
Trader Joes Imported English Authentic Lemon Curd, 10.5oz (300g), 24 jars/case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trader Joes Company
FDA (openFDA food enforcement)
Reported Mar 8, 2017
BD AffirM VPIII Microbial Identification Test
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Mar 8, 2017
Check-Flo Performer Introducer, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 8, 2017
DR Systems Unity PACS software, now known as Merge Unity PACS. Product Usage: Merge Unity PACS is a medical image and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Mar 8, 2017
Abdominoplasty Pack, Part numbers AMS3326(B, AMS4381, and AMS4381(B.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Windstone Medical Packaging, Inc.
123 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 1, 2017
Trader Joe's Harvest Whole Wheat Bread; NET WT 24 oz. (1 lb. 8 oz.) SKU 00132; UPC: 0000 1328. Distributed and sold…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Athens Baking Company
FDA (openFDA food enforcement)
Reported Mar 1, 2017
A) Palmer's Candies Chocolate Almond Bark , NET WT 9 OZ (255 g) packaged in plastic clamshell container, UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Palmer and Company, dba Palmer Candy Co.
17 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 1, 2017
Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience, Inc.
FDA (openFDA device enforcement)
Reported Feb 22, 2017
Burts British Hand Cooked Potato Chips Sea Salt & Malted Vinegar 150gx10 and 40gx20
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bwi Inc.
FDA (openFDA food enforcement)
Reported Feb 22, 2017
Fratelli Beretta USA, Inc. Recalls Mortadella Product Due To Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fratelli Beretta USA, Inc.
USDA FSIS
Reported Feb 22, 2017
LIFEPAK 15 Monitor, Automated External Defibrillator (AED), Manual mode monitoring and therapy functions are intended…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported Feb 22, 2017
CentraLink¿ Data Management System Software Versions: v13x,v14x,v15x The CentraLink system software is a network…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Celerity ECG Cable Accessory Pack, STERILE, Rx ONLY - distributed under the following labels: (a) angiodynamics…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics Inc. (Navilyst Medical Inc.)
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Boston Scientific, EMBLEM S-ICD Programmer Model 3200 Programmer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Feb 8, 2017
Raley'ss Canned Cut Green Beans 14.5oz ; UPC: 4656700204
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raley's
FDA (openFDA food enforcement)
Reported Feb 1, 2017
FRONT: Stauffer's Animal Crackers Original; Net Wt. 32 OZ.; BACK: (best by date): 07SEP17; (bag lot numbers) LC120716…
High riskUsing this product could cause serious injury, illness or death — stop using it now.D. F. Stauffer Biscuit Co., Inc.
FDA (openFDA food enforcement)
Reported Feb 1, 2017
SCC Soft Computer Softbank II software Product Usage: Supports single and multi-site transfusion services in healthcare…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Soft Computer Consultants, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 25, 2017
Halo One 5F Introducer Sheath 45 cm Product Code: HAL545 The Halo One Thin-Walled Guiding Sheath is designed to perform…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bard Peripheral Vascular, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 25, 2017
Ambra PACS UDI: +AMBRHEALTHSOLUTIONS0/$$+7_V3.16.13.0R Software Version Number: V3.16.13.0 Intended for use as a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dicom Grid Inc.
FDA (openFDA device enforcement)
Reported Jan 25, 2017
Monaco RTP System. Used to make treatment plans for patients with prescriptions for external beam radiation therapy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
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.