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.

2,548 stored notices name Nevada, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Nevada too — those are in the archive.

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)

Medical devices

Reported Jun 18, 2025

Newport HT70 Ventilator, REF: HT70M-JP-NA, HT70M-CN-NA, HT70M-ES-EU, HT70M-PT-BR, HT70M-SY-EU, HT70M-WW-EU,…

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

Covidien

FDA (openFDA device enforcement)

Medical devices

Reported Jun 18, 2025

IVENIX INFUSION SYSTEM LVP Blood Products Administration Set, Dual-Inlet, Low-Sorbing, Y-Site, Mesh Filter, 15 mL.…

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

Fresenius Kabi USA, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 11, 2025

Sample probe sucks a sample dispensed into a tube or cup and discharges the appropriate amount into a cuvette. Lot…

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

Beckman Coulter Mishima K.K.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 11, 2025

Fresh & Ready Foods Breakfast Bistro Box, 4 oz. plastic container. Best buy: 05/09/2025-05/12/2025 UPC# 6 82906 89908 9

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

Fresh & Ready Foods LLC

85 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 11, 2025

GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet contains four tablets and a capsule. Paper-board carton that…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

GNC Holdings LLC

FDA (openFDA food enforcement)

Food

Reported Jun 11, 2025

Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gummies (120 gummies/bottle); 12 bottles/case

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Nordic Naturals, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 4, 2025

Atellica IM Homocysteine Calibrator (2 Pack). Siemens Material Number: 10995498

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)

Medical devices

Reported Jun 4, 2025

Plus Initial Drill, Article Number: 103.170;

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

Straumann USA LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 4, 2025

Ultrasonic Cleaning Systems Triton 36 Model Number 6003000804 Triton 72 Model Number 6003000805 Ultrasonic cleaning…

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

Ultra Clean Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 28, 2025

Bard Minnesota Four Lumen Esophagogastric Tamponade Tube, REF:0092220 18 Fr. (6mm, 7/32"), 41" Length (104cm) with 8"…

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

C.R. Bard Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 28, 2025

PhenoMATRIX

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

Copan WASP

FDA (openFDA device enforcement)

Medical devices

Reported May 28, 2025

META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690

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

Smith & Nephew, Inc.

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.