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 48,100 notices were distributed nationwide, so they reach Nevada too — those are in the archive.

Medical devices

Reported Jul 20, 2022

PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System, Catalog numbers PG2990BPS, PG2990BPX,…

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

Cordis US Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

HAMILTON-H900 Humidifier, Models: 950001, 950004

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

Hamilton Medical AG

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

MiniMed 620G Insulin Pump (O.U.S. version)

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

Medtronic MiniMed

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Peak Universal Bond Self-Etch Bottle Kit, Part: 4541; Peak Universal Bond Self-Etch Intro Kit, Part: 4554; Peak SE…

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

Ultradent Products, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Endo Model Modular Rotational Tibia - Small (Model No #15-2814/02), Medium (Model No #15-2814/03), and Large (Model No…

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

Waldemar Link GmbH & Co. KG (Mfg Site)

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

CoolMax ZELTIQ Vacuum Applicator REF BRZ-AP1-080-000

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

Zeltiq Aesthetics, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

Omnera 400T Digital Radiographic System

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

Arcoma AB

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

Palindrome Precision Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic…

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

Covidien LLC

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2022

Yukon Straight Rod 4.0 x120mm; Cat# 7601-540120. Used to provide immobilization and stabilization of spinal segments.

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

K2M, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2022

Volcano Visions PV. 035 Digital IVUS Catheter REF 88901, PN: 300005384002 Rx Only, Sterile EO, CE 2797

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

Volcano Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 29, 2022

Mini Peanut Butter Cream Pie. Product was available for purchase at the following banner: Haggen. Packaged in clear…

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

Albertsons Companies LLC

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 29, 2022

REF: PIG1260K, 6Fr, X10, Safe-t-Centesis Catheter drainage Kit, Sterile EO,

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 29, 2022

BVI Wet -Field Eraser, 18GA Blunt Tip, 45Deg.-Intended to remove tissue and control bleeding by the use of high…

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

Beaver Visitec International, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 29, 2022

Trader Joe's BBQ & Black Pepper Toscano Chopped Salad 11 oz. Contains Milk, Soy, Wheat Dist. & Sold Exclusively By:…

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

Taylor Farms Retail Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 22, 2022

Drager SafeStar 55, Catalog No. MP01790

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

Draeger Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 22, 2022

Cobalt Models loaded with CareLink SmartSync Device Manager application software D00U005: a) Cobalt XT VR: DVPA2D1,…

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

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 22, 2022

Thistle Watermelon Berry Cold-Pressed Organic Juice watermelon strawberry lime chia 32 FL OZ (355 mL) Keep Refrigerated…

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

Thistle Health Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 15, 2022

SUPPLE BEARS QUERCETIN BROMELAIN GUMMIES + Vitamin C & Zinc 60 DIETARY SUPPLEMENTS NO SOY, NO GLUTEN, NO EGGS, NO…

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

6174 Industries, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jun 15, 2022

Back up batteries in Ventilators labeled as the following: a. CARESCAPE R860 Ventilators (K142679) b. ENGSTROM…

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

GE Healthcare, LLC

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 15, 2022

Triathlon Tritanium Tibial Component (Size 6); Catalog Number 5536-B-600 Triathlon¿ Tritanium¿ Tibial Component (Size…

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

Howmedica Osteonics Corp.

FDA (openFDA device enforcement)

Food

Reported Jun 15, 2022

Pimlico Confectioners Vegan Fine Hazelnut Truffles in a 3.88-ounce green plastic package.

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

The TJX Companies, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 8, 2022

In-Line ventilator adaptor

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

Baxter Healthcare Corporation

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 8, 2022

JIF CREAMY PEANUT BUTTER packaged in 18gram, 500gram, 1 kilogram, 1.1oz (120 count)12oz, 16oz, 28oz, 40oz, 48oz, 4lb…

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

The JM Smucker Company LLC

23 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 8, 2022

Jason & Mary Large Milk Peanut Butter Cup

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

Walnut Creek Chocolate Co. Inc.

14 more products in this recall

FDA (openFDA food enforcement)

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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.