All recall categories

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 Mar 6, 2024

IdentiTi ALIF Standalone Interbody System: Part Number/Description 132-10-85-250 / IdentiTi ALIF SA Graft Bolt, 08.5 x…

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

Alphatec Spine, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 6, 2024

Chin Jung White Kimchi - 3 lb. 8 oz (1.58 kg) plastic jars

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

Chin Jung Corporation

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 6, 2024

Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, REF 46913, Sterile EO, Rx Only. Used…

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

Medtronic Neurosurgery

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 6, 2024

MUTTI Crushed Tomatoes; Polpa; Net Wt 27.9 OZ (1lb 11.9 OZ) 790g; UPC 85469300071

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

Mutti USA Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 6, 2024

Tensive Conductive Adhesive Gel, Product Ref. 22-60. 12, 1 case contains 12 inner boxes with 50g tubes packaged in each.

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

Parker Laboratories, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 6, 2024

Marketside Southwest Chopped Kit 10.3 oz. UPC 681131305129

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

Ready Pac Foods Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 6, 2024

Cotija cheese packaged in the following configurations: 1. Sargento Course Grated Cotija Cheese Pack Size 6/5 lb.…

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

Sargento Foods, Inc.

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 6, 2024

USTAR II Hip System Press-Fit Curved Stem, RHS Ti Plasma Spray for the following reference numbers: REF: PE11151211 -…

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

United Orthopedic Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 28, 2024

HENRY SCHEIN¿ CRITERION¿ EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-2448)

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

AMD Medicom Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 28, 2024

Baxter Exactamix Pro 1200, REF EXM12DY

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

Baxter Healthcare Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 28, 2024

Meta Psyllium Fiber Capsules packaged as 100 count or 160 count PET bottles - 12 bottles per case.

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

The Procter & Gamble Company

FDA (openFDA food enforcement)

Medical devices

Reported Feb 21, 2024

BIOFIRE Blood Culture Identification 2 (BCID2) Panel when used with: BD BACTEC Lytic Anaerobic medium BD BACTEC Peds…

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

BioFire Diagnostics, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2024

global Medium, Model Numbers LGGG-020 (20mL bottle), LGGG-050 (50mL bottle), LGGG-100 (100mL bottle). Intended use:…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2024

Samsung Digital Diagnostic Mobile X-ray System, Model GM85.

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

NeuroLogica Corporation

FDA (openFDA device enforcement)

Food

Reported Feb 21, 2024

Dragonfly Jelly Bar Handbag 11.64oz, 17.63oz UPC Code 721557357156, 721557357163 Dragonfly Jelly Bar Backpack 7.93oz,…

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

U.S. Tov, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 21, 2024

3:1 Dermacarrier, Model Number 00219501300, skin graft carrier

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

Zimmer Surgical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 14, 2024

FilmArray Pneumonia Panel Plus (Pneumoplus), REF: RFIT-ASY-0143, CED 2797, IVD, Rx Only (30 test kit)

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

BioFire Diagnostics, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 14, 2024

Sperm separation media are used to separate motile sperm from other constituents of semen.

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

Fujifilm Irvine Scientific, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 14, 2024

Guardian 4 Glucose Sensor, REF: MMT-7040A, MMT-7040C1, MMT-7040C2, MMT-7040C3, MMT-7040D1, MMT-7040D2, MMT-7040MA,…

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 14, 2024

Total immunoglobulin M (IgM total) IVD, kit, nephelometry/turbidimetry

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 14, 2024

Dual Articulating Headrest, Pad Ret P/N P141210805, REF BF754

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

Steris Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 7, 2024

Notoginseng Formula Special Gout Granule; 100% Natural; 8 G x 10 PACKS; CITI TRADE INT'L LIMITED; ADDRESS:…

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

8th Ave Pharmacy

FDA (openFDA food enforcement)

Medical devices

Reported Feb 7, 2024

MB362R - JACOBSON DUROGRIP TC Micro Needle Holder, straight, 8 3/4", (220 mm), "TC JACOBSON NDL HLD STR JAW 220MM";

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

Aesculap Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 7, 2024

Surgilon Braided Nylon sutures: 88861919-31 SURGILON* 4-0 BLK 7X75CMPCT 88861919-41 SURGILON* 3-0 BLK 7X75CMPCT…

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

Covidien LP

1 more product in this recall

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.

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.