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 Feb 11, 2026

COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in…

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

Beckman Coulter, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 11, 2026

JUICE from the Raw, DETOX GREENS

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

Everpress Juice

6 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 11, 2026

Brand Name: Da Vinci Product Name: da Vinci X, Xi Surgical System, & da Vinci 5 Surgical System Model/Catalog Number:…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 11, 2026

Product is Frozen Half Shell Oysters in 15-16 pound blocks. Packaged in generic brown cardboard boxes. Side panel…

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

Khee Trading, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 11, 2026

MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software Version 6.60 The MiniMed 780G insulin pump…

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 11, 2026

CINNAMON POWDER NET WT : 3.5 oz (100g) PRODUCT OF INDIA UPC 7 46241 29537 8 Distributed by: Venzu Traders LLC…

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

Venzu Traders LLC

FDA (openFDA food enforcement)

Food

Reported Feb 11, 2026

WinCo Foods Deli Margherita Pizza Thin Crust, Item #67279. Net wt. 17oz. UPC 0267279 807987. Product is Take & Bake and…

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

WinCo Foods LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 4, 2026

PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010

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

Cerapedics, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 4, 2026

McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g), packaged as an 84-count carton, UPC 043000073438.…

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

Keurig DR Pepper, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 4, 2026

Conductivity Standard Solution Catalog/Model Numbers: 10001, 10011, 10021, 10032, 10040, 10040c, and 10041 Conductivity…

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

NIPRO Technical Services, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 4, 2026

Butternut Squash Tamales With Roasted Green Chiles, Corn & Jack Cheese Ingredients: Organic Corn Flour Masa, Organic…

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

Prima Vera Nueva, Inc.

9 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 4, 2026

Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count bottle, BIO7772 120 count…

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

Quten Research Institiute LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jan 28, 2026

The LDL-Cholesterol assay is comprised of two distinct phases. In phase one a unique detergent solubilizes cholesterol…

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

Beckman Coulter Ireland, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 28, 2026

SQ40S Blood Transfusion Filter

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

GVS TM, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 28, 2026

Tego Connector: REF: 011-D1000, 01C-D1000, 055-D1000, D1000; Conector Tego: REF: LAT-D1000

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

ICU Medical, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 28, 2026

Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Bag Model/Catalog Number: 490127 Software Version:…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 28, 2026

Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Reference Numbers: ENDO-AN2030/B IN4130/CNK IN4130/H…

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

Merit Medical Systems, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 21, 2026

FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre 3 sensor is a component of the…

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

Abbott Diabetes Care, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 21, 2026

VANTAGE GALAN 3T Model MRT-3020/MEXL-3020

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

Canon Medical System, USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 21, 2026

Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is intended for the qualitative detection in…

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

Diagnostica Stago, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 21, 2026

Fran s PureBar Almondmilk Chocolate 46% Madagascar Plant-Based, net wt. 1.1oz, UPC 7 49668 24280 2. Ingredients: Sugar,…

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

Fran's Chocolates Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 21, 2026

Ivenix Infusion System (IIS), LVP Software: LVP-SW-0005.

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

Fresenius Kabi USA, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 21, 2026

da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073 (2.7-4cm,SP1098, Box) & 430075…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 21, 2026

CentriMag Blood Pump, REF: 102953, 201-20003, 201-90010, 201-90016; CentriMag RVAD HDE KIT, REF: 104318; CentriMag…

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

Thoratec 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.