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 Dec 20, 2023
Acorn Raspberry Creme Filled Cookie found in gift basket: #067 Believe Cookie, Cake and Brownie Collection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Houdini Inc.
8 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 20, 2023
Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 781350. Philips Magnetic Resonance (MR)…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips North America LLC
FDA (openFDA device enforcement)
Reported Dec 20, 2023
Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 RX REF 420-159 Spectranetics Turbo-Elite Laser Atherectomy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
FDA (openFDA device enforcement)
Reported Dec 13, 2023
BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, used with Maine Molecular Quality Controls,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Dec 13, 2023
Whole cantaloupe 3ct and 6ct brand name Imperial Fresh
High riskUsing this product could cause serious injury, illness or death — stop using it now.Freshpoint Of Southern Ca
FDA (openFDA food enforcement)
Reported Dec 13, 2023
Freedom Boom models series: F110, F120, F130, F320, F330, F350, F410, and F420 with built in 42A Lightweight Spring Arm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ihb Operations B.v.
FDA (openFDA device enforcement)
Reported Dec 13, 2023
EVO+VISIAN Implantable Collamer Lens, REF:VICM5_12.1. Phakic Intraocular lens.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Staar Surgical Company
10 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 13, 2023
NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176
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 Dec 6, 2023
Acumen IQ Sensor, REFs: AIQS6, AIQS65, AIQS6R, AIQS6R5, AIQS8, AIQS85, AIQS8R5, Rx only, Sterile EO. For use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syringe adapter Smallbore…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
FilmArray TORCH REF HTFA-ASY-0104. HTFA-ASY-0104 is the BIOFIRE TORCH Base which includes barcode scanner, touch screen…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Nov 29, 2023
EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Outer box UPN# M0054242CE0.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
Ventlab, LLC AirFlow manual resuscitator devices with integrated manometer, multiple accessory configurations to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SunMed Holdings, LLC
8 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 22, 2023
AU/DxC AU Chemistry Transferrin REF: OSR6152 Immune complexes formed in solution scatter light in proportion to their…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Biomedical Division
FDA (openFDA device enforcement)
Reported Nov 22, 2023
Takumi brand frozen tuna ground meat, raw but ready to eat, vacuum packaged units in fiber boxes, net wt. 11 lbs. per…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tokai Denpun USA Inc.
FDA (openFDA food enforcement)
Reported Nov 15, 2023
Similac Probiotic Tri-Blend - 0.017oz (0.50g) packaged in foil packets. 50 foil packets per carton - 3 cartons per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA food enforcement)
Reported Nov 15, 2023
BREG REF 100519-000 WALKER FOLDING WALKER WITH WHEELS Utilized as a walking aid.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Breg Inc.
FDA (openFDA device enforcement)
Reported Nov 15, 2023
BD Alaris PCU REF 8015
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 15, 2023
CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT, SKU 900260
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Family Dollar Stores, Llc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 15, 2023
Gills Onions 3 lb. bags, diced yellow onions
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gills Onions, LLC
72 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 15, 2023
StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The StealthStation System, with StealthStation…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Nov 15, 2023
Philips EPIQ Diagnostic Ultrasound System Models: EPIQ 7G(model # 795200), EPIQ 7C (Model # 795201), EPIQ 7W (Model #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 15, 2023
Zephyr Endobronchial Valve (EBV) 5.5-LP, REF: EBV-TS-5.5-LP
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pulmonx, Corp.
FDA (openFDA device enforcement)
Reported Nov 8, 2023
AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM, REF: 45-751324
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microvention Inc.
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Nevada recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.