Skip to main content

Recalls in Nevada

Recalls sold in Nevada, including nationwide recalls, newest first.
Agency
Risk level
Date
Sold in

16 recalls

Children's Tiny Land Play Tents

Children's Tiny Land Play Tents have fiberglass poles that can shed fibers, causing skin and eye irritation.

CPSC, Injury hazard

Vornado SRTH Small Room Tower Heaters

The fan blade can detach, causing overheating and melting that can ignite and pose a fire hazard.

CPSC, Fire hazard

IC Bus CESB School Buses

The wheelchair restraint retractors on certain IC Bus CESB school buses may not lock, allowing the wheelchair to move and increasing injury risk.

NHTSA, Mobility equipment defect

Jeep Wrangler, Wrangler 4XE and Gladiator Vehicles

The electric hydraulic power steering pump wiring may overheat and cause a vehicle fire, even when parked.

High risk, NHTSA, Fire risk when parked

Chrysler Pacifica (2020-2022)

The battery pack may cause a vehicle fire, even when parked, increasing injury risk.

High risk, NHTSA, Fire risk when parked

Acura MDX (2014-2020), Honda Passport (2019-2023), Honda Pilot (2016-2022), and Honda Ridgeline (2017-2023)

Rear suspension components may fail in certain Honda and Acura vehicles, causing loss of control and increasing crash risk.

NHTSA, Vehicle structure defect

Honda Accord Hybrid (2023-2026), Honda CR-V Fuel Cell EV (2025-2026), and Honda CR-V Hybrid (2023-2026)

Tire repair kit bottle caps may detach, becoming a projectile and striking people nearby.

NHTSA, Tire defect

10 recalls

Lannett Niacin Extended-Release Tablets

Niacin Extended-release Tablets failed dissolution specifications during stability testing.

Moderate risk, FDA, Drug dissolving problem

Guardian Drug Antacid Tablets

Antacid tablets contain small metallic particles.

Moderate risk, FDA, Foreign object

Forte BioPharma Xyvona (Levorphanol Tartrate Tablets)

Xyvona (levorphanol tartrate tablets) has a labeling issue and is not marketed under the proprietary name.

Moderate risk, FDA, Labeling error

Asclemed USA Duloxetine DR Capsules

Duloxetine DR Capsules contain a nitrosamine impurity above the acceptable limit.

Moderate risk, FDA, Drug impurity

Fresenius Kabi Ivenix Infusion System LVP Software

The LVP software of the Ivenix Infusion System can report a false battery-health value and trigger a battery-depletion alarm.

High risk, FDA, Software defect

CareFusion 303 BD Pyxis Medication Cabinets

BD Pyxis medication cabinets have a fingerprint scanner that may overheat and cause first-degree burns.

Moderate risk, FDA, Device defect

B. Braun Spinal Needle Procedure Kits

Spinal Needle procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP, with potential quality issues.

High risk, FDA, Device defect

Entegra Qwest SE, Condor, Jayco Granite Ridge, and Melbourne Recreational Vehicles

The taillight warning light may incorrectly illuminate on the instrument panel display, potentially causing confusion and increasing crash risk.

NHTSA, Electrical system defect

2026 Entegra Qwest and Jayco Melbourne Prestige Recreational Vehicles

The taillight warning light may incorrectly illuminate on the instrument panel display, potentially causing confusion and increasing crash risk.

NHTSA, Electrical system defect

Aston Martin Valkyrie

The Aston Martin Valkyrie has a brake master cylinder seal that can deform, causing overheated brakes and a fire risk.

NHTSA, Brake defect

11 recalls

Prime Food Processing Dried Herring Fish

Dried Herring Fish may be improperly eviscerated, which can lead to botulism poisoning.

High risk, FDA, Botulism

Spectra Medical Devices Lidocaine HCl Injection

Lidocaine HCl Injection USP may lack sterility.

Moderate risk, FDA, Sterility problem

Albertsons: 121 products

Albertsons foods contain undeclared allergens.

Moderate risk, FDA, Undeclared tree nut

Sato Yunker Energy & Health Herbal Supplement with Vitamins

This herbal supplement with vitamins does not meet label claim for Vitamin E.

Low risk, FDA, Wrong nutrient levels

Ascend Laboratories Amlodipine and Olmesartan Medoxomil Tablets

Amlodipine and Olmesartan Medoxomil Tablets have failed dissolution specifications, with olmesartan medoxomil content below specifications.

Moderate risk, FDA, Drug dissolving problem

Shimadzu Digital Angiography and Radiography Systems

Digital Angiography Systems and a Digital Radiography System have electromagnetic contactors that may weld together.

Moderate risk, FDA, Device defect

Braun Ram ProMaster Seat Belts

Wheelchair seat belts may have incompatible connectors and fail to properly restrain occupants, increasing injury risk in a crash.

NHTSA, Seat belt defect

Kia Telluride and Kia Telluride Hybrid (2027)

The driver seat belt strap may not extend, failing to restrain an occupant in a crash and increasing injury risk.

NHTSA, Seat belt defect

Braun Chrysler Pacifica and Voyager Vehicles

Air bags may not deploy in certain Chrysler Pacifica and Voyager vehicles, increasing the risk of injury in a crash.

NHTSA, Air bag defect

Nova Bus LFS (1997-2002, 2005-2024) and Nova Bus LFS Artic (2009-2014, 2016-2024)

Nova Bus LFS transit buses have a low brake air pressure warning light that may fail to illuminate when the engine is off, increasing crash risk.

NHTSA, Brake defect

Daavlin Phothera 200 Phototherapy Devices

Phothera 200 Phototherapy Devices have calibration certificates with reversed outputs.

Moderate risk, FDA, Device defect

4 recalls

CASE v7.0 Cardiac Testing System

The CASE v7.0 Cardiac Testing System can spark at the printer head, potentially causing serious thermal injury.

Moderate risk, FDA, Device defect

Covidien EndoStitch Polysorb Single Use Loading Unit

The Covidien EndoStitch Polysorb Single Use Loading Unit may have holes in its pouch, compromising the sterile barrier.

Moderate risk, FDA, Sterility problem

Grand Design Reflection Fifth Wheel Recreational Trailers

Reflection fifth wheel trailers have shock bolts that may be incorrectly tightened, and broken parts can become a road hazard.

NHTSA, Suspension defect

Philips Azurion 3M12, 3M15, 5M12 and Other Angiography Systems

Philips Azurion systems may show a dark image during Roadmap Pro, not clinically usable.

Moderate risk, FDA, Device defect

8 recalls

Motor City Pizza Co. 5 Cheese Bread

Motor City Pizza Co. 5 Cheese Bread may be contaminated with Salmonella, which can cause serious infections.

Moderate risk, FDA, Salmonella

Eugia Lidocaine HCl Injection

Lidocaine HCl Injection has a label wrap that covers the barcode, making it hard to scan.

Low risk, FDA, Labeling error

Fresenius Kabi Ivenix Infusion System (IIS), Large Volume Pump

The Ivenix Large Volume Pump can be damaged by dropping or jarring, causing unintended touchscreen behavior.

High risk, FDA, Device defect

Exacta Mix Vented Micro-Volume Inlet

Exacta Mix Vented Micro-Volume Inlet tubing sets may contain incorrect filters, causing reduced flow and clinical effects.

Moderate risk, FDA, Device defect

Becton Dickinson & Company BD Spinal Trays

BD Spinal Trays with Quincke or Whitacre needles have quality deficiencies related to acceptance testing.

High risk, FDA, Device defect

Fresenius Kabi Ivenix Infusion System Large Volume Pump

The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS) has a cassette loading lever that can break.

Moderate risk, FDA, Device defect

Forest River Salem (2024-2026), Forest River Stealth EVO (2026), and Forest River Wildwood (2024-2026)

The fireplace outlet may have incorrect wiring, increasing the amperage and risk of a fire.

NHTSA, Vehicle equipment defect

Mercedes-Benz GLE, GLS and Maybach Vehicles

The rear seat belt bolts may not be tightened properly, and a loose belt may not restrain an occupant during a crash.

NHTSA, Seat belt defect

17 recalls

MiniWarGaming and Primal Horizon Disc Magnets

Disc magnets violate the mandatory safety standard, posing a deadly ingestion hazard to children.

CPSC, Swallowing hazard

Panasonic-Branded Lithium Coin Batteries

The coin batteries are not in child-resistant packaging and lack required warning labels, which can cause serious injuries if swallowed.

CPSC, Swallowing hazard

Anzmtosn Luminous Fidget Spinner Balls

Luminous Fidget Spinner Balls have easily accessible button cell batteries that can cause serious injury or death if swallowed.

CPSC, Swallowing hazard

Misco Sports Light-Up Racket Sets

If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.

CPSC, Swallowing hazard

Mainstays 9-Drawer Fabric Dressers

Mainstays 9-Drawer Fabric Dressers are unstable if not anchored, posing tip-over and entrapment hazards that can cause serious injury or death to children.

CPSC, Tip-over hazard

Medtronic 1x4 and 2x4 Pocket Adaptor Kit for Deep Brain Stimulation

The Medtronic Pocket Adaptor Kits are labeled with incorrect Use-By-Dates.

Moderate risk, FDA, Labeling error

Medline Anesthesia and Spinal Trays

Medline kits containing Huons Bupivacaine in Dextrose Injection have quality issues, including data integrity concerns and efficacy complaints.

High risk, FDA, Device defect

Philips Azurion and Allura Systems

The Azurion system may show decreased performance as it ages, potentially causing loss of imaging functionality.

Moderate risk, FDA, Device defect

Better Weather Actives Fix Elixir

Better Weather Fix Elixir may contain undeclared Mitragynine and Mitragynine Pseudoindoxyl, which can cause nausea, vomiting, and other effects.

FDA

ARBOC Specialty Vehicles Spirit of Equess (2025) and 3 more

The wheelchair restraint retractor may not lock, allowing the wheelchair to move during transit.

NHTSA, Mobility equipment defect