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 Oct 2, 2013

Dannon ACTIVIA¿ LIGHT Nonfat Yogurt Strawberry-Banana & Peach Flavor, 12 PACK of 4oz cups, Form fill seal 4oz cup

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

The Dannon Company, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 25, 2013

3M Scotchcast, Wet or Dry Cast Padding, Catalog Numbers WDP2, WDP3, WDP4, and WDP6. Intended for use in constructing…

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

3M Company - Health Care Business

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2013

Blanketrol III, Model Number 233, Cincinnati Sub-Zero Products, Inc., 12011 Mosteller Road, Cincinnati, OH 45241…

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

Cincinnati Sub-Zero Products Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 25, 2013

Pills bury Cinnamon Rolls with Icing, CINNA BON, USPC 1800000501, 1800052230, 12.4 oz and 2-pack USPC 1800045675,2-…

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

General Mills, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 25, 2013

ACL TOP (Base); PN 0000280000 Bench top, fully automated, random access analyzer designed specifically for in vitro…

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

Instrumentation Laboratory Co.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2013

Cranial Access (CRAK) Kits, Product / Catalogue No.s: INSHITH, INSHITHND, INSHITHRZN The kits allow for access to the…

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

Integra LifeSciences Corp. d.b.a. Integra Pain Management

FDA (openFDA device enforcement)

Food

Reported Sep 25, 2013

Fresh Basil (Sweet Hawaiian and Thai) New Dream Team Inc. HI

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

New Dream Team

FDA (openFDA food enforcement)

Medical devices

Reported Sep 25, 2013

Brilliance CT 6, M/N 728256; Brilliance CT 16 M/N 728246; Brilliance CT 40, M/N 728235 & Brilliance CT 64 M/N 728231,…

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 Sep 25, 2013

Responder 5 is a nurse call communication system that connects patients with staff in a hospital. The nurse call system…

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

Rauland-Borg Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 18, 2013

*** 1) Cat. 4341B; Qty. 10; Thoracentesis Tray; With Catheter; Sterile; CareFusion; 1500 Waukegan Road; McGaw Park, IL…

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

Carefusion 2200 Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 18, 2013

First Street Coffee Cake Muffins (S 45398) 4 count 14 oz. UPC 0 4151210848 8

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

KDK Management, Inc., dba Bubbles Baking Co.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 18, 2013

Tempa DOT Single-Use Clinical Thermometer Medical Indicators Made in U.S.A. by Medical Indicators, Inc. 16 Thomas J…

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

Medical Indicators, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 18, 2013

ADVIA Centaur Folate (100 Tests), SMN 10310308, Cat No. 06367974 In vitro diagnostic use in the quantitative…

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

Siemens Healthcare Diagnostics, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2013

Boston Scientific, Small Peripheral Cutting BalloonTM, Sterilized using irradiation: The Peripheral Cutting Balloon…

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

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 11, 2013

Kroger Break 'N Bake Chocolate Chip Cookie Dough, refrigerated dough, packaged in 16.0 oz. plastic package.

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

Conagra Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 4, 2013

3M ESPE Unitek Primary Stainless Steel Crowns (First Primary UL4), Product code 902150 (Kit- 112 crowns/kit) and 900114…

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

3M Company/3m Espe Dental Products

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2013

DeRoyal Insufflation Tubing sets: 1) REF 28-0206 Insufflation Tubing, Laparoscopic Rx Only 2) REF 28-0214 Hi-Flow…

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

DeRoyal Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2013

Pipeline Embolization Device (PED) The Pipeline Embolization Device is indicated for the endovascular treatment of…

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

Micro Therapeutics Inc., dba Ev3 Neurovascular

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2013

Synthes 2.4mm VA-LCP Two Column Volar Distal Radius Plate and Torque limiting attachment, 1.2Nm Synthes VA-LCP Distal…

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

Synthes (USA) Products LLC

FDA (openFDA device enforcement)

Food

Reported Sep 4, 2013

Trois Comtois Morbier Cheese labeled as follows: Morbier Raw Milk PLU 293358; Morbier AOC Le Trois PLU 293608; Morbier…

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

Whole Foods Market

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 28, 2013

Evviva Fresh Peach Spumante, UPC 84279-99137

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

Johnson Brothers Liquor Company, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 21, 2013

GE LightSpeed CT750 HD The GE LightSpeed CT750 HD Computed Tomography X-ray system is intended to produce…

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

GE Healthcare, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2013

Colorimetric (CM)/ Rate (RT) incubator wear pads. Product Codes: 1) 6801375, 2) 6801890, 3) 6802445, 4) 6802413 Product…

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2013

Remel X/pect Flu A&B Control Swabs, For In Vitro Diagnostic Use, Ref R246003, each package contains 20 Flu A Control…

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

Remel 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.