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.
2,546 stored notices name Nevada, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Nevada too — those are in the archive.
Reported Dec 24, 2025
Orthofix NorthStar OCT Navigation Surgical Technique Guide, and instruments: Navigation Driver, REF: PC2-400012;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Seaspine Orthopedics Corporation
FDA (openFDA device enforcement)
Reported Dec 17, 2025
Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer System Model/Catalog Number:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Orthofix U.S. LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 10, 2025
Blonde Beard's Dojo Asian Wing Sauce, wing sauce hot sauce condiment, shelf stable, 2 years, glass bottle, 8 oz, Blonde…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blonde Beard's
FDA (openFDA food enforcement)
Reported Dec 10, 2025
InSure ONE Fecal Immunochemical Test. Labeled as follows: 1. Insure ONE POL Patient Kit - 10 pack. Model Number: 90010.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Enterix, Inc.
FDA (openFDA device enforcement)
Reported Dec 10, 2025
Genepro Whey 4th Generation Plasma Treated Protein, unflavored, Net Wt. 225g, 30 servings, packaged in a resealable…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Genepro Protein, Inc.
FDA (openFDA food enforcement)
Reported Dec 10, 2025
Low-moisture part-skim mozzarella shredded cheese, individually packaged in a plastic bag, as: 1) Always Save -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Great Lakes Cheese Co. Inc.
6 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 10, 2025
Phantom Fibula Nail, 2.8mm x 130mm, Right, Ti, Fibula Nail, REF: P36-128-130R-S
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paragon 28, Inc.
FDA (openFDA device enforcement)
Reported Dec 10, 2025
Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound, LLC
FDA (openFDA device enforcement)
Reported Dec 3, 2025
CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K, Description/REF: 25+ TOTALPLUS CP PAK 20K CPM BWV .9 IU/…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research LLC
FDA (openFDA device enforcement)
Reported Dec 3, 2025
Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
FDA (openFDA device enforcement)
Reported Dec 3, 2025
FoundationOne CDx (F1CDx), RAL-0003 version 31.0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Foundation Medicine, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2025
CareLink Clinic, REF: MMT-7350
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Dec 3, 2025
Nat's Nuts Cinnamon Whiskey Pecans, 4 oz.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nats Nuts LLC
FDA (openFDA food enforcement)
Reported Nov 26, 2025
BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Nov 26, 2025
REF: CC286297 or BS737162 Automated Digital Cell Morphology analyzer DI-60, IVD in conjunction with a Honeywell Vuquest…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cellavision AB
FDA (openFDA device enforcement)
Reported Nov 26, 2025
PhD Hemostasis Valve, REF: IN4802/K, IN4802/T, IN4918/A, IN7802/C, IN8802/C, IN9802, IN9802/A, K05-02166B, K05T-02138A,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Nov 19, 2025
CEREPAK Detachable Coil System - Name/REF: UNIFORM 2MM X 2.5 CM/FCX100202, UNIFORM 2.5MM X 3.3 CM/FCX100253, UNIFORM…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cerenovus Inc.
FDA (openFDA device enforcement)
Reported Nov 19, 2025
Carton Label: PACIFIC FRESH VEGETABLES PACIFIC INTERNATIONAL MARKETING SALINAS, CA 93912 Carton Sticker Label: Conv…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pacific International Marketing
3 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 19, 2025
Product Name: Nutra Calm Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 90, Dose: 2 Capsules. Product Sku:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Professional Botanicals, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 19, 2025
Ceiling Type X-Ray Tube Support Models CH-200 and CH-200M used with RADspeed, SonialVision and FLUOROspeed Systems The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Corporation Medical Systems Division
FDA (openFDA device enforcement)
Reported Nov 19, 2025
Multichem ID-B. Model/Catalog Number: SR103B Intended for use as an unassayed positive qualitative quality control…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Techno-Path Manufacturing Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 12, 2025
Brand Name: Leksell Stereotactic System Product Name: Leksell Vantage Stereotactic System Software Version: n/a Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Nov 12, 2025
Tandem Mobi Insulin Pump: Description/Catalog: Tandem insulin pumps are battery-operated infusion pumps capable of both…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tandem Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported Nov 5, 2025
VANTAGE GALAN 3T. CMSC Model: MRT-3020/U7. Model Number: MEXL-3020/B7.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
FDA (openFDA device 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.