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.
Reported Dec 14, 2016
McConnell's Fine Ice Cream Dutchman's Chocolate
High riskUsing this product could cause serious injury, illness or death — stop using it now.McConnell's Ice Cream, Inc.
6 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 14, 2016
Miravalle Pan Rallado Bread Crumbs Net Wt. 7 oz., 8 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Miravalle Foods, Inc.
FDA (openFDA food enforcement)
Reported Dec 14, 2016
Brilliance 64 728231 Computed Tomography X-ray systems intended to produce cross-sectional images of the body by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2016
Taylor Farms Veggie & Hummus Bistro Box: Baby Carrots, Hummus Dip, Grape Tomatoes, Flatbread squares, Celery Sticks.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Taylor Farms Pacific Inc. (MacArthur Facility)
FDA (openFDA food enforcement)
Reported Dec 7, 2016
ConforMIS iTotal Cruciate Retaining (CR) Knee Replacement System, Sterile Catalog Number: TCR-111-1111. Intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConforMIS, Inc.
FDA (openFDA device enforcement)
Reported Dec 7, 2016
Monaco RTP System; Used to make treatment plans for patients with prescriptions for external beam radiation therapy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 30, 2016
COBRA Fusion 50 Ablation System, COBRA Fusion 150 Ablation System, and COBRA Fusion Magnetic Retriever System. Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
LIAISON Estradiol II Gen, 310680, 310680-CN The DiaSorin LIAISON Estradiol II Gen assay is a chemiluminescent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diasorin Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
Philips Healthcare System X-ray Tomography Computed :
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 23, 2016
Version 1.2.0 of Accu-Chek Connect Diabetes Management App (iOS) released on July 11, 2016
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2016
RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Nov 16, 2016
Zimmer¿ Air Dermatome II Handpiece Loaner, item number 01-8851-001-00. Device is packaged inside of a padded-foam…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
DM Light Slices Yellow Cling Peaches -15 oz (425g) 300 x 407
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Del Monte Research Center - Walnut Creek
FDA (openFDA food enforcement)
Reported Nov 2, 2016
ReTurn 7500/7500 Aid, transfer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Handicare USA, Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
Keystone Dental PrimaConnex¿ Straight Implant TC, RD Internal Connection 4.0 x 11.5mm. Product code:15613K Implants are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keystone Dental Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
Neptune Plus (Hemostatic Pad), Part Numbers: 8870-03 Neptune Pad is used to promote the rapid control of bleeding and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TZ Medical, Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Awareness Boost Tea Dietary Supplement Passion Fruit Net Wt 7.4 oz. Distributed by & for all inquiries: Awareness…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Awareness Corporation
FDA (openFDA food enforcement)
Reported Oct 26, 2016
Endoscopic Articulating Linear Cutter, ATB35. Standard 35 MM. The ENDOPATH ETS-Flex Endoscopic Articulating Linear…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 26, 2016
COZY SHRIMP, 200 CT, Prepared by: Kabobs, 54234 North Lake Dr. Lake City, GA 30260.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kabobs Inc.
26 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 26, 2016
Nature's One, Organic PediaSmart¿ Dairy Vanilla complete nutrition beverage for kids 1 to 13 years NET WT 12.7 oz (360…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natures One Inc.
FDA (openFDA food enforcement)
Reported Oct 26, 2016
OER-Pro Endoscope Reprocessor, Endoscope washer/disinfector
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Oct 26, 2016
LipiFlow thermal Pulsation System, consisting of Console and Activator, Model LFD-1100 The LipiFlow Thermal Pulsation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tearscience, Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Abdominoplasty Pack, Kit number AMS3326 convenience custom kits used for general surgery in hospital operating room
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Windstone Medical Packaging, Inc.
149 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Calix P PEEK Lumbar System, PLIF Rasp
Moderate riskThis product could cause temporary or reversible health problems — stop using it.X Spine Systems Inc.
3 more products in this recall
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.