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 Sep 7, 2022

Metalogix Self-Drill Half-Pin, a component of the Revolution External Fixation System. Orthopedic. Metalogix Self-Drill…

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

New Standard Device Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 31, 2022

Organic Amaranth Grain Gluten Free, Bob's Red Mill brand, packaged in Standup Pouch (24oz). Each case consists of 4/24…

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

Bob's Red Mill Natural Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 31, 2022

DeRoyal limb holders: (1) DeRoyal Limb Holder, Wrist, Fixed, Quick Release, REF M8124; (2) DeRoyal Limb Holder, Ankle,…

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

DeRoyal Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

(1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (2) GE Centricity Universal Viewer 7.0, Model 5826659-0XX;…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable…

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

Medtronic Neuromodulation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 24, 2022

Ready Meals Shrimp Cooked with Cocktail Sauce SCE NET WT 12 OZ CAL 330 NET WT. 0lb 12oz (340g) ready2eat Tomato paste,…

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

Albertsons Companies LLC

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 24, 2022

Marutomo Dashi Soup Base, Item # #37402 Ingredients: Dried Shaved Skipjack Tuna, Fish Extract (Dried Skipjack Tuna,…

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

Wismettac Asian Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 17, 2022

The Cholestech LDX¿ System combines enzymatic methodology and solidphase technology to measure total cholesterol, HDL…

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

Alere San Diego, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 17, 2022

Clear American brand "Strawberry Punch Snow Cone" flavored sparkling water beverage with other natural flavors; 1-liter…

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

Refresco Beverages US Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 17, 2022

cobas e801 Immunoassay Analyzer

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10

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

Aesculap Implant Systems LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit (ESU) designed to be used with the da Vinci Xi and…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

SARS CoV 2 rapid antigen test kits packaged under the following brands: Oral Rapid Test, Oral Rapid Antigen Test, SML…

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

North American Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

Merlin PCS 3650 programmer Model 3330 software

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

St. Jude Medical, Cardiac Rhythm Management Division

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 10, 2022

Vicks Children's Botanicals Liquid Daytime/Nighttime Combo Pack 4oz plastic bottles

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

The Procter & Gamble Company

4 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 10, 2022

Amaranth Grain Organic, brand Natural Grocers, packaged in plastic bag, net wt. 1 LB (454g) UPC 0 00080 12550 1. Label…

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

Vitamin Cottage Natural Food Markets, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 3, 2022

REF: 4P52-20 Hemoglobin A1c for use with Architect, IVD, CE, R1 1 x 52 mL, R2 1 x 20 mL, A1cDL 2 x 35 mL

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

Abbott Laboratories

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 3, 2022

Bumble Bee Smoked Clams Shucked Easy Open NET WT. 3.75 oz. (106 g) Distributed By: Bumble Bee Seafoods San Diego, CA…

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

Bumble Bee Foods, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 3, 2022

Centricity PACS Software Version 7.0 SP0.0.4.7

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 3, 2022

Da Vinci S/Si Large Clip Applier, Model 420230 Da Vinci S/Si Medium-Large Clip Applier, Model 420327 Da Vinci S/Si…

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

Intuitive Surgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2022

BD Connecta Stopcock with OFF Directed Tap Without Extension Tube (500 eaches/carton) Catalog No. 394910 (US)

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

Becton Dickinson & Company

10 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2022

LifeGlobal Fast Freeze Thawing Kit, Model No. GFT5-055

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2022

LumiraDx SARS-CoV-2 Antibody (Ab) Test Strip

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

LumiraDx

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2022

SX-One MicroKnife

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

Sonex Health 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.