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 48,122 notices were distributed nationwide, so they reach Nevada too — those are in the archive.

Food

Reported Sep 24, 2014

Swanson 100% Certified Organic, Carob Powder, Raw Chocolate Substitute, Net wt 1 lb (454 grams), in round 1000 cc High…

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

Swanson Health Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 17, 2014

The BD MAX MRSA Assay, catalogue #442953. An automated qualitative in vitro diagnostic test for the direct detection of…

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2014

PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin Stapler (Model PRR35), PROXIMATE PX Fixed-Head Skin Stapler…

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

Ethicon Endo-Surgery Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2014

Life Force Chamber Product Usage:The product is intended for restful contemplation and spirituality.

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

Life Force

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2014

Prime Care ¿ Transcend Mattress, Prime Care ¿ Transcend Perimeter Mattress, Prime Care ¿ Transcend Advanced Mattress,…

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

Primus Medical LLC

FDA (openFDA device enforcement)

Food

Reported Sep 10, 2014

Brown carob powder packed in a plastic heat sealed 16oz. bag, labeled in part "Live Superfoods Carob Powder***NET WT 16…

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

Live Superfoods

FDA (openFDA food enforcement)

Medical devices

Reported Sep 10, 2014

EN MENTOR Round High Profile Single Use Saline Breast Implant Sizer Single Use Saline Breast Implant Sizer REF…

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

Mentor Texas, LP.

FDA (openFDA device enforcement)

Food

Reported Sep 10, 2014

Organic Carob Powder; Certified Organic, Product of Italy. Store in Cool, Dark place. Packaged in 16 oz., 5 lb., 20 lb…

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

River Canyon Retreat

FDA (openFDA food enforcement)

Food

Reported Sep 10, 2014

Organic Carob Powder, 1 lb., 20 lb., and 55 lb. bags Expiry date: 6/5/2015, UPC Code 803813-04429-8

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

Sunfood Superfoods

FDA (openFDA food enforcement)

Medical devices

Reported Sep 10, 2014

PERSONA The Personalized Knee System Constrained Tibial Articular Surface Provisional BOTTOM with the following: L CD…

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

Zimmer, Inc.

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 3, 2014

CloverSnare 4-Loop Vascular Retrieval Snare. Product is packaged in a Tyvek-film sterilizable outer package and is…

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

Cook Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 3, 2014

ORGANIC TRADITIONS SPROUTED CHIA SEED POWDER NET WT. 8 oz. and 16 oz., UPC 854260006162, item number AHM616 and UPC…

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

Health Matters America Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 27, 2014

American Spoon Food Sour Cherry Marmalade, 9.5 oz in glass jars with metal lid e. Total package size (e.g. 12 packages…

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

American Spoon Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 27, 2014

Vanguard 360 Femoral Boss Reamer, Label: REF 32-488474 VANGUARD 360 1NSTRUMENT FEMORAL BOSS REAMER NON-STERILE, BIOMET…

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

Biomet, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 27, 2014

Philips IP5 Information Portal The Expression Information Portal (Model IP5), a display and device controller for…

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

Invivo Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 27, 2014

TomoTherapy Treatment System, Model: Hi-Art, Catalog/Part Number: H-0000-0003, software versions 1.2.0, 1.2.1 and 1.2.2…

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

TomoTherapy Incorporated

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 27, 2014

Gelweave (TM) Vascular Prostheses Manufactured by - VASCUTEK Ltd a TERUMO company

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

Vascutek, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 27, 2014

Magna-Fx Cannulated Screw Fixation System Bone Screw Fully Threaded Sterile zimmer

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

Zimmer, Inc.

15 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2014

Esaote PA230E Transducer A portable and cart base ultrasound system for general and cardiovascular imaging

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

Biosound Esaote, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2014

Codman Certas - In Line Valve Only; Product Code: 82-8800 The Codman Certas Programmable valve is an implantable device…

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

Codman & Shurtleff, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2014

IntelliSpace Portal (ISP) DX/HX/EX, IntelliSpace Portal (ISP) IX, and IntelliSpace Portal (ISP) LX SPECT IntelliSpace…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 13, 2014

VIDAS TPSA, in vitro diagnostic, for use as an automated quantitative measurement of prostate specific antigen levels…

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

BioMerieux SA

FDA (openFDA device enforcement)

Medical devices

Reported Aug 13, 2014

Sonopet Ultrasonic Surgical System Console, Ultrasonic Aspirator, Stryker Medtech.

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

Stryker Instruments Div.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2014

Horizon Medical Imaging It is a medical image and information management application that is intended to receive,…

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

Mckesson Medical Immaging

FDA (openFDA device enforcement)

Free recall alerts

Get alerted about new Nevada recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

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.