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 Jul 30, 2025

ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL

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

Johnson & Johnson Vision Care, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 30, 2025

Sushi Wasabi; 5 grams (Ready to eat) Ingredients: Horseradish, Corn Oil, Salt, Water, Citric Acid, Tumeric, FD&C Blue#1…

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

Ming Hong International Inc.

FDA (openFDA food enforcement)

Food

Reported Jul 30, 2025

Ritz Peanut Butter Cracker Sandwiches, Net Wt.27.6 oz, 20 count (20x1.38 oz) 6- pack of cracker sandwiches inside…

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

Mondelez Global LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 30, 2025

Azurion 7 M20. Fluoroscopic X-Ray System.

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

Philips Medical Systems Nederland B.v.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2025

Stryker, StrykeFlow , REF: 0250070500, 2, Disposable Suction/Irrigator without Disposable Tip

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

Stryker Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 30, 2025

SunBiotics Activated Almonds Infused with Probiotics, Oat Milk Chocolate, NET WT. 1 oz(28g) packaged in cases.

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

Windy City Organics LLC

FDA (openFDA food enforcement)

Food

Reported Jul 23, 2025

Red cabbage, shredded packed in polybag and cardboard case. 14 lbs per case.

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

And Go Concepts dba Salad and Go

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 23, 2025

SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve, REF: SCXT3-5-2000; SwabCap, 200-ct. Box, REF: SCXT3-2000

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

ICU Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 23, 2025

i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.

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

Intersurgical Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 23, 2025

Chocolate Crunch Cake Bar (85000), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master…

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

Rich Ice Cream Co.

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 16, 2025

Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Vitrectomy Procedure Pak Model/Catalog…

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

Alcon Research LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 16, 2025

Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI16 Software…

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

Edwards Lifesciences, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 9, 2025

--- Shell Eggs; Brown; Various sizes - medium, large, and jumbo; Various pack sizes - 5, 12, 18, and Loose ---- Clover…

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

August Egg Company

FDA (openFDA food enforcement)

Medical devices

Reported Jul 9, 2025

REF: 335775 , BD FACS, 7-Color Setup Beads, 25 setups per kit, Rx Only, IVD. Used in flow cytometry for fluorescence…

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

Becton, Dickinson and Company, BD Bio Sciences

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 9, 2025

BD Heyman Follower Straight Tip for following sizes: 10Fr - REF:21110, 12Fr - REF:21112, 14Fr - REF: 21114, 20Fr - REF:…

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

C.R. Bard Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 9, 2025

HardyCHROM CRE, selective and differential culture medium for antimicrobial susceptibility testing, Product Catalog No.…

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

Hardy Diagnostics

FDA (openFDA device enforcement)

Food

Reported Jul 9, 2025

Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12, 24,…

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

Peak Cocktails

FDA (openFDA food enforcement)

Medical devices

Reported Jul 2, 2025

REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487; B92488; C24317; C28652; C37500; D04164;…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

REF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA X 1.00 IN (0.9 X 25 MM) 35mL/min, STERILEEO, RxONLY

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

Becton Dickinson Infusion Therapy Systems, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

Product Name [REF]: Supply Server, CCE Enterprise SW Site License (2-5), BD Pyxis Logistics [806], BD Pyxis MedStation…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 25, 2025

GCE HEALTHCARE Zen-O lite, Portable Oxygen Concentrator, Model RS-00608-X-S

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

Ohio Medical Corporation

FDA (openFDA device enforcement)

Food

Reported Jun 25, 2025

Topo Chico MINERAL WATER CARBONATED 16.9 FL OZ (500mL) Bottle UPC 0 21136 18061 9, Case UPC 0 21136 18062 6 MADE IN…

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

The Coca-Cola Company

FDA (openFDA food enforcement)

Food

Reported Jun 25, 2025

Great Plains Bentonite + Herbal Detox Capsules 60 capsules, packaged in PETE amber bottle, white plastic cap and tamper…

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

Yerba Prima Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 18, 2025

Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium With Priming Cap Back Check Valve 2 SmartSite…

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

Bd Switzerland Sarl

4 more products in this recall

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.