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 Aug 4, 2021

ThermoScientific Oxoid Antimicrobial Susceptibility Discs Rx only Made in the United Kingdom

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

Remel Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 4, 2021

Zippie Voyage, early intervention stroller - Product Usage: is manually operated by a caregiver for purposes of…

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

Sunrise Medical (US) LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 28, 2021

Infant Heel Warmer with Attachment Tab, Nonsterile, Active Product SKU MH00002T The infant heel warmer is activated at…

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

Cardinal Health 200, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 28, 2021

Circle K Chicken Salad Sandwich, 5.9 oz. (167g) clamshell packaging with tamper strip, UPC 815138013996, Manufactured…

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

Lsg Sky Chefs

FDA (openFDA food enforcement)

Medical devices

Reported Jul 28, 2021

Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10. The Respironics V60/V60 Plus Ventilator is an…

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

Respironics California, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 21, 2021

Toshiba Vantage Tiitan 1.5T with Standard gradient, Premium Open-Bore MRI System, REF: MRT-1504 - Product Usage: use as…

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

Canon Medical System, USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 21, 2021

Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Sterile EO Rx Only

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

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

FDA (openFDA device enforcement)

Medical devices

Reported Jul 21, 2021

Lingen Disposable Virus Sampling Kit, Item MTM-04, 40 tubes/box.

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

Mercedes Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 14, 2021

FilmArray Pneumonia Panel (Pneumo) Part Numbers: Part No: RFIT-ASY-0144 / UDI: 00815381020178 (30 test kit) Part No:…

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 Jul 14, 2021

Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model Number: 20-006-024

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

Luminex Corporation

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 14, 2021

CoreValve Evolut R Delivery Catheter System, REF: ENVEOR-L; ENVEOR-N;

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

Medtronic Heart Valves Division

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 7, 2021

5Fr PowerPICC Catheter Single-Lumen with 70cm Guidewire Instructions For Use: PowerPicc Polyurethand Radiology PiCC…

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

Bard Access Systems Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 7, 2021

Synaptive Trackable Suction Set Standard and Malleable

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

Synaptive Medical Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 30, 2021

a.) Banner Smoked Fish Inc. brand Sliced Smoked Scotch Style Salmon (Salmon, Salt, Sugar, Natural Wood Smoke, Sodium…

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

Banner Smoked Fish Inc.

35 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 30, 2021

Concord Farms Fresh Enoki Mushrooms; 5.25 oz. (150g) or 7 oz. (200g) packages UPC: 049995041049 and 04999504103 US…

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

Concord Farms

FDA (openFDA food enforcement)

Medical devices

Reported Jun 30, 2021

inLight Medical LED Pads used with Polychromatic light technology system

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Inlightened Partners LLC

FDA (openFDA device enforcement)

Food

Reported Jun 30, 2021

Tight! Xtreme Reloaded: 120 count capsules (serving size 3 capsules) Ingredients: Evapor8 Total Body Fat Assault Matrix…

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

SAN Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Jun 23, 2021

GE Healthcare Innova IGS 3 (GTIN 00840682147378), Innova IGS 5 (GTIN 00840682124621), Innova IGS 6 (GTIN…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 23, 2021

OSSUR MIAMI J SELECT COLLAR - Product Usage: is intended to provide gross immobilization to the cervical spine. REF:…

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

Ossur Americas

FDA (openFDA device enforcement)

Medical devices

Reported Jun 23, 2021

Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 CPU is also used as spare part.

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

Radiometer Medical ApS

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 16, 2021

COVID-19 Self-Test Kit *** INNOVA *** 7T

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

Innova Medical Group, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 16, 2021

Normand Remisol Advance Data Manager is a software device that interfaces between laboratory information systems (LIS)…

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

Normand-Info S.A.S.U.

FDA (openFDA device enforcement)

Food

Reported Jun 16, 2021

Chicken Street Taco kit in a plastic tray with a clear plastic lid.

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

The Kroger Co.

FDA (openFDA food enforcement)

Food

Reported Jun 9, 2021

Lipodrene With 25mg Ephedra Extract 100CT UPC 8 57084 00056 9

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

Hi Tech Pharmaceuticals

FDA (openFDA food 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.