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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.

Medical devices

Reported May 14, 2014

Nonabsorbable Surgical Suture, U.S.P., Sterile - Do Not Resterilize, Deknatel. Indicated for use in soft tissue…

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

Teleflex Medical

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 7, 2014

Abbott Acclaim Infusion Pump Designed to deliver parenteral infusions including whole blood or red blood cell…

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

Hospira Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2014

The CEP 8 SpectrumGreen (SG) ASR Probe Kit, 20ul (list 06J37-018) is an Analyte Specific Reagent (ASR) containing a…

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

Abbott Molecular

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2014

Amo-O Herbal Stimulator, 2 fl. oz. Manufactured by Meta Labs, Alpharetta, GA 30076, UPC Code 80702-1 Product Usage: The…

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

Altasource LLC dba Meta Labs LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2014

ZYM B Reagent (REF 70493). The ZYM B reagent is an additional test used to reveal the results of some miniaturized…

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

BioMerieux SA

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 30, 2014

Sprouts Farmers Market Organic Whole Black Peppercorns, 2.12oz., UPC Code 8-74875-00425-4, Lot Numbers 3287 and 3246.…

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

Sprout's Farmers Market

FDA (openFDA food enforcement)

Medical devices

Reported Apr 30, 2014

Stryker PenAdapt"; Rx Only, Sterile. This device is an accessory to an electrosurgical unit (ESU). The PenAdapt is used…

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

Stryker Instruments Div.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2014

SmartSite Extension Set, Model No. 20029E, intravascular administration set.

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 23, 2014

Luna Chocolate Chunk; Whole Nutrition Bar for Women; 15 count box. Clif Bar & Company, Emeryville, CA

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

Clif Bar And Company

FDA (openFDA food enforcement)

Food

Reported Apr 23, 2014

Strawberry Fruit Bar, 3 oz., Helados La Tapatia Fresno, CA 93706

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

Helados La Tapatia, Inc.

52 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Apr 23, 2014

Simply Lite brand 50% CaCao Low Carb Sugar Free Dark Chocolate (NET WT 3 oz (85g), packaged in a brown plastic foil…

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

Simply Natural Foods LLC

FDA (openFDA food enforcement)

Medical devices

Reported Apr 16, 2014

Playtex Nurser Deluxe Double Electric Breast Pump, Model X06578AO, powered by a 12V DC power supply, Model SY-12120,…

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

Energizer Personal Care

FDA (openFDA device enforcement)

Food

Reported Apr 16, 2014

Evolution fresh Organic sweet Greens and Ginger, 15.2 fluid-ounce bottle, 6 bottles/case, UPC code is 762357378927.

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

Evolution Fresh Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 9, 2014

Ideal Protein Double Chocolate Brownie. Individually wrapped, sold in boxes of 7.

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

Laboratories Cop Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 9, 2014

Kirkland Signature brand Real Sliced Fruit, Item # 527069. The UPC on the master cardboard case is 0 96619 52706 9.…

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

Oregon Freeze Dry Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 9, 2014

Pinnacle3 Radiation Therapy Planning (RTP) System, software version 9.0.

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 Mar 26, 2014

Dental Abutment labeled in part: "4555 Riverside Drive Palm Beach Gardens, FL 33410 USA 1-800-342-5454***EDAZ , EDAZx…

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

Biomet 3i, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 26, 2014

High Mowing Organic Sprouting Seeds Ancient Eastern Blend , 4 oz. resealable plastic bag UPC Code: 872724005445

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

High Mowing Organic Seed

FDA (openFDA food enforcement)

Medical devices

Reported Mar 26, 2014

2.5MM Aggressive Blade Known as a Sinuscopic Shaver Blade, this device is composed of a metal cutter and plastic drive…

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

Stryker Instruments Div.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

Treatment packs used on the VisuMax Laser Keratome. Size M Manufactured by Carl Zeiss Meditec AG, Jena, Germany. The…

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

Carl Zeiss Meditec AG

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

XiO RPT System The XiO RTP System is used to create treatment plans for any cancer patient for whom external beam…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

GE Healthcare, Innova 2100IQ, Innova 3100, Innova 3100IQ, Innova 4100, Innova 4100IQ Innova 2121IQ, Innova 3131IQ;…

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

GE Healthcare, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

Smith & Nephew RENASYS Soft Port REF: 66800799 (The RENASYS Soft Port Dressing Kits are used in conjunction with…

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

Smith & Nephew Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

4040-2: Umbilical 3 mL Line Draw, Luer lock syringe (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ device,…

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

Smiths Medical ASD, Inc.

12 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.