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 Apr 1, 2020
VNS Therapy Programmer, Model 3000 used with Models 103, 104, 105, 106, or 8103 VNS Therapy generators.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Medline Stick Sponge Presaturated W/PVP REF DYND70288 DYND70288H 2/PK Expiration 06/30/2022.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Whole Foods Market Green Chile Chicken Tamale served as a Family Meal, Chef's Case, Packaged, Frozen and on he hot bar…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market
FDA (openFDA food enforcement)
Reported Apr 1, 2020
WinCo Foods frozen Blackberries, item # 107414, packaged in polyethylene bags, with a net weight of 16 oz (1 lb or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Winco Foods LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 25, 2020
Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avid Medical, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 25, 2020
Outshine Fruit Bars Strawberry; 6 Fruit Ice Bars; 14.7 Fl. oz. (435 mL) UPC: 041548610047 Case UPC: 10041548610044
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dreyers Grand Ice Cream, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 25, 2020
IMMULITE 1000 Systems E2 Estradiol Catalog #: US: LKE21(D) and OUS: LKE21 - Product Usage: For in vitro diagnostic use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2020
Monoject 3mL Syringe with Hypodermic Safety Needle, 22G x 1-1/2 . Item Code 11832215 - Product Usage: used for general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2020
Butterfly Shrimp 16/20, 50 lb. cases
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Les Chateaux De France
FDA (openFDA food enforcement)
Reported Mar 18, 2020
Sunny Select Au Jus Gravy Mix 1 OZ pouch (24 pouches per case)
High riskUsing this product could cause serious injury, illness or death — stop using it now.McCormick & Company, Inc. - Flavor Manufacturing Center
FDA (openFDA food enforcement)
Reported Mar 18, 2020
GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2020
SoundWave Professional Suite Software 3.2, Ref CI-6055-014, SPN 058-023-32085, UDI: (01)07630016853227, Logical…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Advanced Bionics, LLC
FDA (openFDA device enforcement)
Reported Mar 11, 2020
Enzymatic Creatinine Reagent (CR-E 2 X 200), REF A60298, For in Vitro Diagnostic Use, Rx Only, UDI: 15099590625733
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 11, 2020
Blendtopia Superfood Smoothie Kit Glow flavor, 7 oz flexible pouch
High riskUsing this product could cause serious injury, illness or death — stop using it now.Blendtopia Products, LLC
4 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 11, 2020
CareFusion Alaris System, Alaris PC unit models 8000 and 8015 (UDI: 10885403801518)
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 11, 2020
Remisol Advance running on hardware with Windows XP, Windows 7, Windows Server 2003 and Windows Server 2008 operating…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Normand-Info S.A.S.U.
FDA (openFDA device enforcement)
Reported Mar 11, 2020
Seca 402/403 Baby Scale Cart, Ref # 4020000009/ REF # 4030000009
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Seca
FDA (openFDA device enforcement)
Reported Mar 11, 2020
Natural Grocers Organic Extra Virgin Coconut Oil, packaged in glass jars with metal lids and a plastic shrink seal,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vitamin Cottage Natural Food Markets, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 4, 2020
COHERENCE Oncologist, Model Nos. 07333680 & 07351898
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Feb 26, 2020
UST-2265-2 Probe, Part Number: UST-2265-2 - Product Usage: The UST-2265-2 probe is intended to be used for diagnostic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Feb 26, 2020
SnapLink, Ref Part No. 438-2190, L6R SnapLink, Slot .022, TQ--28, Ang +2, Rot +2, Qty 10, Made in Mexico, CE 0086, Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ormco/Sybronendo
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
bliss anti-stress formula Dietary Supplement, 60 Tablets; Manufactured For and distributed by: Market America, Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Market America Inc.
FDA (openFDA food enforcement)
Reported Feb 19, 2020
Medtronic MiniMed 630G System with SmartGuard, Ref/Model # MMT-1515, MMT-1715, MMT-1714, MMT-1754, and MMT-1755 *US and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Button-Style Tocotransducer (Nautilus), 8-foot Cord 2264HAX, that may have been serviced with the following: Pacific…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacific Medical Group Inc.
9 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.