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 Nov 8, 2017
Whole Foods Hand Pie Apple Cinnamon 3 PK, NET WT 8 oz. PLU number 23646100000
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market
4 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 1, 2017
Intralipid 20%, A 20% I.V. Fat Emulsion, 100 ml bag, Rx only, Manufactured by Fresenius Kabi, Uppsala, Sweden for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baxter Healthcare Corporation
FDA (openFDA drug enforcement)
Reported Oct 31, 2017
FSIS Issues Public Health Alert for Poultry Products Due To Possible Listeria Contamination
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Ghiringhelli Brothers
USDA FSIS
Reported Oct 18, 2017
waterfront Bistro Tatar Sauce, Net Wt 9 oz. (255g), UPC 21130-12242
High riskUsing this product could cause serious injury, illness or death — stop using it now.Silver Spring Foods, Inc.
FDA (openFDA food enforcement)
Reported Oct 11, 2017
Simplot Traditional Tater Gem. Net Wt. 30 lb. (13.6 kg), foodservice corrugated case, 6/5 lbs. clear poly bags per…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.J R Simplot Co. Corporate HQ
FDA (openFDA food enforcement)
Reported Oct 11, 2017
Bio35, Vitamin-Mineral Omega Oils Trace Minerals Dietary Supplement, 100 Softgel Capsules. UPC 0-26341-12900-2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pro Bioteks Laboratories
FDA (openFDA food enforcement)
Reported Sep 27, 2017
Spine Referencing Instrumentation, Spinous Process Clamp, Tall When used with a Medtronic StealthStation Navigation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 20, 2017
Phentermine, USP Capsules, 15 mg, 30 count bottles, Rx only, Packaged By: Aidarex Pharmaceuticals, Corona, CA, MFG:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Aidarex Pharmaceuticals LLC
FDA (openFDA drug enforcement)
Reported Sep 20, 2017
Spectra-System/Legacy Guided Surgery Handle Kit, Device Listing Number D245883. The Guided Handle Kit (G-HK) allows…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Sep 20, 2017
Cell Marque, Podoplanin (D2-40 Mab), 7 mL, REF PA0796, IVD, The antibody is intended for in vitro diagnostic (IVD) use.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Biosystems Richmond Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 20, 2017
Makoplasty Partial Knee Application (PKA) Product Usage: The Robotic Arm Interactive Orthopedic System (RIO) is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 13, 2017
MOSAIQ Medical Charged-Particle Radiation Therapy System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Sep 13, 2017
Southeastern Mills, Biscuit Gravy Mix, Net Wt. 2.75oz (77g), 4.5oz (128g) flexible plastic packages.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Southeastern Mills Custom Seasoning Solutions
5 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 6, 2017
Alere iScreen Dx Urine Drug Screen Card, 20 Drug Detection, Kit Contents include 26 individually pouched devices and 1…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ameditech Inc.
FDA (openFDA device enforcement)
Reported Sep 6, 2017
UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System, Software Version 3.2. The DxH Slidemaker Stainer allows…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Sep 6, 2017
iVue with Normative Database, Device Listing Number D185549. Product Usage: The iVue (K121739) is a non-contact, high…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Optovue, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 30, 2017
DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation (DBS) lead kits, models 3387/3387S, 3389/3389S, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Aug 30, 2017
Tissu-Trans Filtron 100, 3-TT-FILTRON 100. Product Usage: Intended for fat transfer and liposuction.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shippert Medical Technologies
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 23, 2017
Arctic Sun 5000 Temperature Management System, 100-120 V North America and 100-120 V US
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Aug 23, 2017
VNS Therapy¿ AspireHC¿ Generator, VNS Therapy¿ AspireSR¿ Generator. Model No. 105. Product Usage: United States…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cyberonics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 23, 2017
Truliant Tibial Trial Handle. To assist the surgeon in the implantation of Truliant Knee system components according to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Aug 9, 2017
Professional Formulas Sublinqual B12 High-Potency dietary supplement, 60-count dissolvable tablet in white plastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Professional Complementary Health Formulas, LLC
FDA (openFDA food enforcement)
Reported Aug 9, 2017
Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid Exchange Catheters Device is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
FDA (openFDA device enforcement)
Reported Aug 2, 2017
North Atlantic Brand - Approx8OZ Raw Breaded Swai Fillet - NET WT. 10lbs (4.54KG)
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Channel Fish Processing Co. Inc.
56 more products in this recall
FDA (openFDA food 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.