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.

Food

Reported Jul 24, 2024

Deluxe Roasted Salted Mixed Nuts ITEM NUMBER 99651 UPC: 6-51433-99651-6 SELL BY: 10/09/2024

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

DSD Merchandisers, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 24, 2024

VACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100 red cap-yellow ring, non-ridged

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

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 24, 2024

Primal Kitchen Avocado Oil 1PT 9.3 FL OZ (750ml) glass bottle UPC 855232007194, 6 bottles per wholesale case

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

Kraft Heinz Foods Company

FDA (openFDA food enforcement)

Medical devices

Reported Jul 24, 2024

QIAcube Connect MDx - IVD Instrument designed to perform automated isolation and purification of nucleic acids in…

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

Qiagen Sciences LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2024

Brand Name: Meridian Angled Awl Fixed Product Name: Angled Awl Fixed Model/Catalog Number: RA2-003015 Product…

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

Seaspine Orthopedics Corporation

FDA (openFDA device enforcement)

Food

Reported Jul 17, 2024

C. Kreuger Gluten Free White Chocolate Cherry Oatmeal Cookies, 2oz in plastic sleeve. 60 cookies per case. Storage for…

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

C. Krueger Finest Baked Goods

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 17, 2024

Kosmos on iOS impacting iOS, Model Numbers: P007639, P007944, software is part of a general-purpose diagnostic…

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

Echonous Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 17, 2024

24K Premium Lense, Distributed by Updream Inc.

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

Ontact Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 17, 2024

9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous…

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

Preat Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 10, 2024

BD Pyxis, Name/REF: MEDBANK MINI 1FH-1FM/ 169-137, MEDBANK MINI 1FH-2HH MEDPASS/ 169-151, MEDBANK MINI 1HH-1FH-1HM/…

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

CareFusion 303, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 10, 2024

Red Button Vintage Creamery Cookie Dough Ice Cream, Net weight 1.75 qt (1.66 L).

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

Casper's Ice Cream, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 10, 2024

Sterile surgical convenience kits: a. Medline Cath Lab Special Procedure, Pack #00-RDF0360, containing a Pure Pouch…

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

MEDLINE INDUSTRIES, LP - Northfield

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 10, 2024

Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade, 35-55mm Model/Catalog Number: MR2102035 Product…

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

Seaspine Orthopedics Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 3, 2024

Tejocote Root Products under the following brands: Eva Nutrition, Science of Alpha Mexican, NWL Nutra Mexican, and…

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

Global Mix Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 3, 2024

Prelude Roadster Guide Sheath REF: -PG4F45S -PG4F90S -PG5F45MP -PG5F45R -PG5F45S -PG5F45S018 -PG5F90MP -PG5F90S…

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

Merit Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 3, 2024

2nd Generation CentriMag Primary Console, REF: 201-90401, 201-90701, 201-90411, 201-90421, 201-30300, L201-90401,…

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

Thoratec Switzerland GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2024

Ventilator HAMILTON-C6, PN: 160021

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

Hamilton Medical AG

FDA (openFDA device enforcement)

Medical devices

Reported Jun 19, 2024

MRI systems: Vantage Orian MRT-1550 (MEXL-1550), Vantage Elan MRT-2020 (MEXL-1520), Vantage Titan MRT-1504 (MEXL-1504),…

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

Canon Medical System, USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 19, 2024

EsoFLIP, 30mm BALLOON DILATION CATHETER, REF ES-330, Rx Only

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

Covidien, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 19, 2024

MyoSPECT System, Model H3912AA and H3912B, and MyoSPECT ES System, Model H3912AB and H3912BD, dedicated cardiac SPECT…

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

Ge Medical Systems Israel, Functional Imaging

FDA (openFDA device enforcement)

Food

Reported Jun 19, 2024

S&S Cup Saimin-Noodles with Soup & Garnish, NET WT. 5 oz., UPC 085315089056 and 085315089070

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

H & U Inc. dba Sun Noodle

FDA (openFDA food enforcement)

Food

Reported Jun 12, 2024

Charles Boggini Pink Lemonde; 1 or 5 U.S. Gallons

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

Charles Boggini Company LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 12, 2024

Leica HistoCore PEGASUS Tissue Processor, REF 14048858005.

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

Leica Biosystems Nussloch GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2024

Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempus LS-Manual User/Operator Manual

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

Remote Diagnostic Technologies Ltd.

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.