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

Medical devices

Reported Jan 26, 2022

VITROS Immunodiagnostic Products High Sample Diluent A Reagent Pack

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

Ortho-Clinical Diagnostics, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 19, 2022

Boba Origin Brown-Sugar Milk Tea 100% WHEY PROTEIN ISOLATE 5.5g BCAA INGREDIENTS: Whey Protein Isolate, Black Tea,…

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

NutraCap Labs LLC

105 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 12, 2022

Simplexa Direct Amplification Disc Kit, Product Kit Code MOL1455

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

DiaSorin Molecular LLC

FDA (openFDA device enforcement)

Food

Reported Jan 12, 2022

Nature's Own Honey Wheat Bread, NET WT 20 oz (1LB 4 OZ) 567g, DISTRIBUTED BY FLOWERS BAKERIES, LLC THOMASVILLE, GA…

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

Flowers Foods (Corporate Offices)

FDA (openFDA food enforcement)

Food

Reported Jan 12, 2022

Trader Joe's Soycutash, Item # 99319. A mix of Sweet Corn, Shelled Edamame, and Red Bell Peppers. Net Wt. 16 oz. (1…

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

Sno Pac Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 5, 2022

iDesign, Model - G300: System AWS (International), System AWS (China), Advanced WaveScan Studio (United States);…

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

AMO Manufacturing USA, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 5, 2022

Karl Storz Udel Sterilization Tray Instructions for Use, Tray Part Number/Description: 39301ACTS/CAMERA TRAY (STERRAD,…

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Jan 5, 2022

ARTISTE with syngo RT Therapist-linear accelerator systems to deliver X-Ray photon and electron radiation for the…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

TruDi NAV Suction Instruments: 0-Degree, REF: TDNS000Z; 70-Degree, REF: TDNS070Z; and 90-Degree, REF: TDNS090Z

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

Acclarent, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

WIRION EMBOLIC PROTECTION SYSTEM, Delivery Catheter and Filter and Retrieval Catheter, 6Fr, REF (Model Number) WRN-D6

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

Cardiovascular Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

Stealthstation System w/ Stealthstation Cranial Software 3.1.1,3.1.2,3.1. or SynergyCranial Software. Synergy Cranial,…

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

Medtronic Navigation, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

Box Label: activ5 TINY GYM IN YOUR POCKET activbody Model: Activ5 User Manual: ACTIV5 USER MANUAL Welcome to Activ5,…

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

Activbody, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

Boston Scientific ROTAPRO, Rotational Atherectomy System Console, Model numbers H74939309010 (US) and H74939309030 (EU).

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

MENTOR Saline-Filled Breast Implants are constructed from room temperature vulcanized silicone elastomer, made of…

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

Mentor Texas, LP.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

Miami J Select Collar, Item: MJS-101, and Miami J Select Collar Set, Item: MJSR-101 Instructions for Use

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

Ossur Americas

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

smith&Nephew EVOS MEDIAL DISTAL FEMUR PLATE, L, 5H, 90MM, REF 72573101

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

Smith & Nephew, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 15, 2021

SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE BIOPSY INSTR 14GA X 9CM; 701114150/SUPERCORE…

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

Argon Medical Devices, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 15, 2021

O3D ORCHESTRATE Orthodontic Technologies User Manual and Data Processing Instructions (model preparation for tooth…

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

Orchestrate Orthodontic Technologies, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 15, 2021

OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 REF 450-0021-00 -OsteoMed D-Power Control…

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

Osteomed, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147 UDI: 00815381020338 Blood Culture Catalog…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 8, 2021

Tastykake Buttercreme Iced Creme Filled Chocolate Cupcakes 14.25oz (6-2ct) box UPC 0 25600 00230 8 & 2.375oz package,…

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

Flowers Foods (Corporate Offices)

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 8, 2021

GE Centricity Universal Viewer Zero Footprint Client

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Number/Product…

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

NuVasive Specialized Orthopedics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

Abbott HeartMate Touch Communication System, REF: HMT1100 (US), HMT1100-R (Rental US), HMT1150 (EU)

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

Thoratec Corp.

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.