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 Sep 24, 2025
FORMUTECH NUTRITION FLEXIBLE JOINT FORMULA WITH CISSUS QUADRANGULARIS SUPPORTS TENDONS & MUSSCLES PROMOTES HEALTH…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hi-Tech Pharmaceuticals Inc.
15 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 24, 2025
CHARGE-UP CHILAQUILES Traditional Mexican breakfast consisting of tortilla chips smothered in a spicy tomatillo salsa…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Itacate Foods LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 24, 2025
Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Max Mobility LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 24, 2025
Pinnacle Radiation Therapy Planning System: Multimodality Simulation Workspace 18.0.5 Model 870258 UDI code:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Sep 17, 2025
Organic BABY bedtime drops; sleep + immunity blend; Promotes restful sleep with natural herbs & supports immunity with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.M.O.M Enterprises, LLC.
FDA (openFDA food enforcement)
Reported Sep 17, 2025
TiBrid Stand Alone Intervertebral Body Fusion Device, SA Angled Punch Awl, Sizes: 30 degree, 45 degree and 60 degree.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Omnia Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 17, 2025
Reef TA Inserter, Part Number: TA2-001003, part of the Reef Interbody System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Seaspine Orthopedics Corporation
FDA (openFDA device enforcement)
Reported Sep 10, 2025
Platelia Toxo IgM Catalog Number 26211 UDI Code: 03610520005552 The Platelia Toxo IgM assay is a semi-quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Sep 10, 2025
Superion IDS Kit Superion Indirect Decompression System 8MM, VF Implant 101-9808 00884662000529 Superion Indirect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Sep 10, 2025
Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number: 31505 Product Description: MediHoney¿…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp. (NeuroSciences)
7 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 10, 2025
Medshape Universal Joints, REF: DNE-9000-UJ
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medshape, Inc.
FDA (openFDA device enforcement)
Reported Sep 3, 2025
BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (N35), REF: 515003 BD PhaSeal Injector Luer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bd Switzerland Sarl
FDA (openFDA device enforcement)
Reported Sep 3, 2025
BD Pyxis Product Name / UDI-DI code / Catalog No. BD Pyxis" MedStation" 4000 Main / 10885403512629 / 303 BD Pyxis"…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Sep 3, 2025
IPC Powerease System REF 2300000 UDI-DI: 00613994448705 00643169406834. The IPC POWEREASE System is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Xomed, Inc.
FDA (openFDA device enforcement)
Reported Sep 3, 2025
Hostess Ding Dongs CHOCOLATE CAKE WITH CREAMY FILLING 2.55 oz twin pack UPC 8 88109 01002 7; 10-1.28 oz carton (12.7…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The J.M. Smucker Company
FDA (openFDA food enforcement)
Reported Sep 3, 2025
Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software Version: N/A Product Description: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.THOR Photomedicine Ltd.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 27, 2025
Burr Hole Cover Kit, REF: M365DB4600C0; Burr Hole Cover Spares Kit, REF: M365DB4605C0. Components of Vercise Deep…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Aug 27, 2025
Product is Frozen Half Shell Oysters in 15 pound blacks. Packaged in generic brown cardboard boxes. Side panel reads:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Khee Trading, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 20, 2025
FG60005 Blueberry Basil Lemonade
Moderate riskThis product could cause temporary or reversible health problems — stop using it.And Go Concepts dba Salad and Go
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 20, 2025
Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner + Tail Large 4 Long X-Ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefree Surgical Specialties
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 20, 2025
Description/REF: BD PYXIS MEDBANK MINI 1FH-1FM/169-137, BD PYXIS MEDBANK MINI 4HM/169-113, BD PYXIS MEDBANK MINI…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Aug 20, 2025
Clover Valley Instant Coffee, NET WT 8 OZ (227 g), packaged in a glass jar, packed 6 jars per case, UPC: 876941004069,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dollar General Corporation
FDA (openFDA food enforcement)
Reported Aug 20, 2025
Sukhi's CLASSIC CURRY PASTE, Net Wt. 2.5 LBS, ITEM # 11-101, UPC: 7-67226-01001-4, SUKHI'S GOURMET INDIAN FOODS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jagpreet Enterprises, LLC. dba Sukhi's Gourmet Indian Foods
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 13, 2025
Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215. for use with IV tubing.
High riskUsing this product could cause serious injury, illness or death — stop using it now.B Braun Medical Inc.
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.