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 Jun 28, 2023
V-Sign Sensor 2, REF VS-A/P/N, a component of Sentec Digital Monitoring System (model SDMS).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SenTec AG
FDA (openFDA device enforcement)
Reported Jun 21, 2023
Driver Instrument, part of the Superion Indirect Decompression System, REF: 102-9800, used with the Superion Indirect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Jun 21, 2023
Tearaway Introducer Kit, REF: KIT-010-12, KIT-010-17, KIT-900-16
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Galt Medical Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 21, 2023
Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F, REF 4992206 Version A, Sterile EO, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 21, 2023
Icelock 125 Ratchet, REF: L-125000; Icelock 600XM Ratchet, REF: L-621200; Icelock 621 Ratchet, REF: L-621000; Icelock…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur H / F
FDA (openFDA device enforcement)
Reported Jun 14, 2023
StealthStation Cranial Software, Models: 9735585, 9735586 (kit), 9735587 (kit), used with StealthStation S7/i7 systems
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)
Reported Jun 14, 2023
Chili Cacahuate Japones, net weight 5 oz (127g), packaged in a soft teal colored plastic pouch with the UPC code 7…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Werner Gourmet Meat Snacks, Inc.
FDA (openFDA food enforcement)
Reported Jun 14, 2023
BencoDental iris 5% NaF varnish, WHITE MINT ITEM # 4323-635; cavity varnish
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Young Dental Manufacturing I, LLC
FDA (openFDA device enforcement)
Reported Jun 7, 2023
Black Fungus Golden Koi 2.5 oz packages 100 bags per case UPC: 81005681145 Product of China
High riskUsing this product could cause serious injury, illness or death — stop using it now.AH USA Group Inc.
FDA (openFDA food enforcement)
Reported Jun 7, 2023
LINK SymphoKnee System L-Shaped Femoral Augment, Medial-Right/Lateral-Left, Sz 5-6 Tilastan, cemented. Intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Linkbio Corp.
FDA (openFDA device enforcement)
Reported Jun 7, 2023
Intelli-C, Right side suspended Tabletop, REF: 03400000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nrt X-Ray A/s
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 31, 2023
Backpacker s Pantry Blueberry Peach Crisp, 4.6-ounce, packaged in a pouch, UPC-048143026143
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Outdoor Products, Inc.
FDA (openFDA food enforcement)
Reported May 31, 2023
Copitas; small ceramic cups; "Del Maguey" embossed on the bottom; distributed by Del Maguey
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pernod Ricard USA Inc.
FDA (openFDA food enforcement)
Reported May 31, 2023
truCONTROL 60 Count
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TruVision Health LLC
11 more products in this recall
FDA (openFDA food enforcement)
Reported May 24, 2023
Beckman Coulter Bicarbonate, REF: OSR6137, 4x25 mL
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 17, 2023
Bard Mission Disposable Core Biopsy Instrument Kit: REF: 2010MSK, 20G x 10CM; REF: 2016MSK, 20G x 16CM
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported May 17, 2023
Ajikal Age Ichiban 97g UPC: 4510656600906
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Daiso California Warehouse
20 more products in this recall
FDA (openFDA food enforcement)
Reported May 17, 2023
Ziyad cinnamon powder, retail 4.5oz plastic jar with shaker cap UPC 074265007432, 12 retail jars per wholesale case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZB Importing LLC
FDA (openFDA food enforcement)
Reported May 10, 2023
Signature Select Oat & Nuts Bread NET WT 20 OZ (1 LB 8 OZ) 680 g Ingredients: Unbleached enriched wheat flour (wheat…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Albertsons Companies LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 10, 2023
LINK SLED Knee System: ENDO SLED KNEE FEM COMP, SMALL Item Number: 15-2020/40
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Linkbio Corp.
47 more products in this recall
FDA (openFDA device enforcement)
Reported May 10, 2023
Ultraview SL (UVSL) Command Module, Model 91496
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Inc.
FDA (openFDA device enforcement)
Reported May 10, 2023
SafeLight Fiber Optic Cable: Clear, 5MM X 10FT 3.05M, REF: 0233-050-100; Gray, 5MM X 10FT 3.05M, REF: 0233-050-200
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
FDA (openFDA device enforcement)
Reported May 3, 2023
(1) Carefusion V. Mueller Graves Vaginal Speculum, Catalog #GL11, Medium Blade, 4 x 1 3/8" (10.2 X 3.5cm); and (2)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
FDA (openFDA device enforcement)
Reported May 3, 2023
HAMILTON-C6, REF: 160021
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hamilton Medical AG
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.