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.
Reported May 4, 2016
Aquilion Lightning CT System iStation cover, SID: 70000246, Item Code: TSX-0354A/2D.03 Product Usage: Aquilion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Apr 27, 2016
Leica Microsystems (Schweiz) Ag. The common name of the device is surgical microscope. It has been assigned the product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Apr 27, 2016
GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12 x4, 6 x12, 1 x 18, 1 x 48, 1 x100, 36 x 4, Mighty Mango Fruit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Materne North America Corp.
16 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 27, 2016
GERBER Organic 2ND FOODS Pears, Carrots & Peas, 3.5 oz., film pouches, 6 pouches per display box/ 2 display boxes per…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle Infant Nutrition
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 27, 2016
iVue and iVue 500 (now called iScan) OCT systems with software version 2016.0.0.127 (USA only) and 2016.1.0.127 (out of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Optovue, Inc.
FDA (openFDA device enforcement)
Reported Apr 27, 2016
Extended Brilliance Workspace NM Nuclear medicine image display and processing application suite. AutoSPECT Pro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 27, 2016
Siemens SOMATOM Definition: Intended to produce cross-sectional images of the body. Computed tomography (CT) x-ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
The Concerto Basic Shower Trolley is intended for assisted hygiene care, especially showering and bathing of residents…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arjo, Inc. dba ArjoHuntleigh
FDA (openFDA device enforcement)
Reported Apr 20, 2016
Arthrex Deltoid Ligament Reconstruction Implant System. Intended as a fixation post, a distribution bridge or for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Apr 20, 2016
Bard TruGuide Disposable Coaxial Biopsy Needle Product Usage: The TruGuide Disposable Coaxial Biopsy Needles are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Apr 20, 2016
GE Healthcare, Aisys CS2 anesthesia..
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
Brilliance 64:Computed Tomography X-ray Systems, Intended to produce cross-sectional images of the body by computer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Device listing number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 13, 2016
TeleSentry Battery, 3.7 Li-Ion Polymer Battery, CAUTION Do not expose to high temperature. Do not disassemble. Dispose…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Scottcare Corporation
FDA (openFDA device enforcement)
Reported Apr 13, 2016
Guardian II Hemostasis Valve, models 8210 and 8211. The following models are only available Outside the US: FH101,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2016
74" (188cm) approximately 9.0ml, 20 Drop Admin Set w/ Integrated ChemoLock Port sterile IV Administration sets are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
The Spectra-System Dental Implant 2008 system is comprised of dental implant fixtures and prosthetic devices that…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Pistachio Raw Whole Shelled 9-oz. retail plastic tub or 5-lb. bulk plastic bag. 12, 9-oz tubs per case. 1, 5# bag per…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipari Foods, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 6, 2016
MAGGI Chicken Flavor Bouillon 6Tab, 12Tab UPC Codes: 028000247959, 028000115678, 028000115678
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle USA
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 6, 2016
Knee Shield (Patella Cup) Product Usage: Knee Shield patella cup is an accessory used with the knee braces to provide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur H / F
13 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Prosupps Dr. Jekyll INTENSE PUMP PRE WORKOUT, 30 SERVINGS, WATERMELON NATURAL AND ARTIFICIAL FLAVOR DIETARY SUPPLEMENT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ProSupps USA LLC
4 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 6, 2016
The E.CAM gamma camera system Product Usage: The E.CAM gamma camera system is a SPECT system and measures the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Cios Alpha, mobile X-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
15 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Synthes Interlocking Bolt, 151 mm (General and Plastics Surgery Devices) Guide, Surgical Instrument
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
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.