The Recall Desk

State

Nevada product recalls

73,366 recalls have nationwide distribution and so reach Nevada. 5,696 additional recalls listed Nevada specifically in their distribution scope.

What the numbers show

Total
5,696
Critical
951
Severe
1,731
Most recent
2026-09-25

Of the 5,696 recalls naming Nevada we have scored against our rubric, 951 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,731 (30%) are Severe.

These figures cover only the 5,696 recalls whose distribution notice names Nevada specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

17776–17800 of 79062

  • SevereNHTSA·23V212000·2023-03-29

    Audi Recalls 2020 Q7 Vehicles Due to Front Camera Fire Risk

    Audi is recalling 2020 Q7 vehicles because a software incompatibility may cause the front camera heating element to overheat, increasing the risk of a fire.

    Product
    AUDI — AUDI Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0633-2023·2023-03-29

    Powdered lemon tea recalled for undeclared milk allergen

    MEITO An extra Stick Powdered Lemon Tea is recalled because the product contains milk that is not declared on the label. Consumers with milk allergies who have purchased this product should not consume it.

    Product
    MEITO An extra Stick Powdered Lemon Tea 5packs UPC: 4902757442804 Made in Japan
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0630-2023·2023-03-29

    Sesame sauce recalled due to undeclared wheat allergen

    Shinsei Additive Free Sesame Sauce is being recalled because wheat allergen was not declared on the product label. Consumers with wheat allergies who consume this product may experience allergic reaction.

    Product
    Shinsei Additive Free Sesame Sauce 22g UPC: 4901665004616 Made in Japan
    Category
    Food
    Distribution
    6 states
  • SevereNHTSA·23V218000·2023-03-29

    Kia Recalls 2015-2019 Soul EV Vehicles for Battery Fire Risk

    Kia is recalling 2015-2019 Soul EV vehicles with E400 batteries because an electrical short-circuit could cause a fire. Owners should contact Kia for a free software update or battery replacement.

    Product
    KIA — KIA SOUL EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0640-2023·2023-03-29

    SENNARIDO pistachio snack recalled for undeclared soy allergen

    DAISO CALIFORNIA WAREHOUSE is recalling SENNARIDO Green Snack Pistachio 90g because the product contains undeclared soy, a major food allergen that poses allergic reaction risk to sensitive consumers.

    Product
    SENNARIDO Green Snack Pistachio 90g UPC: 4974120413421 Made in Japan
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0488-2023·2023-03-29

    Delsam Pharma Artificial Eye Ointment Recalled for Bacterial Contamination

    Delsam Pharma's Artificial Eye Ointment is being recalled for bacterial contamination in unopened tubes. FDA analysis found non-sterility defects in approximately 50,000 units.

    Product
    Delsam Pharma's Artificial Eye Ointment (Mineral Oil 15%, White Petrolatum 83%), 3.5 grams (1/8 oz.) tube, Distributed By: Delsam Pharma Lic, Bronx, Newyork 10469, NDC 72570 122 35, UPC 3 72570 12235 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0642-2023·2023-03-29

    Kurata Menzo Ramen Recalled for Undeclared Coconut Allergen

    DAISO CALIFORNIA WAREHOUSE is recalling Kurata Menzo Meatfree Tonkotsu Ramen Dry due to undeclared coconut on the label. Consumers with coconut allergies who consume this product may experience allergic reactions.

    Product
    Kurata Menzo Meatfree Tonkotsu Ramen Dry 2P 238.8g UPC: 4906436004932 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0636-2023·2023-03-29

    Soft rice crackers recalled for undeclared coconut allergen

    DAISO CALIFORNIA WAREHOUSE is recalling 150YEN HIZATSUKI Soft rice crackers because the product contains coconut that was not declared on the label. Consumers with coconut allergies should not consume this product.

    Product
    150YEN HIZATSUKI Soft rice crackers sea lettuce soy sauce flavor UPC: 4902445210500 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0634-2023·2023-03-29

    Coffee Candy Recalled for Undeclared Coconut Allergen

    Kanro Non sugar coffee candy is recalled because coconut was not declared on the label, posing a risk to consumers with coconut allergies.

    Product
    Kanro Non sugar coffee candy 40g UPC: 4901351013137 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1281-2023·2023-03-29

    Raystation Treatment Planning System Collimator Angle Export Defect

    Raystation radiation therapy planning software may not correctly export collimator angle settings when using the DICOM export function. In exported files, the collimator angle may be replaced with zero regardless of the user's selection.

    Product
    Raystation treatment planning system for radiation therapy, Model Numbers 9.0.0, 9.0.1, 9.1.0, 9.2.0, 10.0.0, 10.0.1, 10.0.2, 10.1.0, 10.1.1, 11.0.0, 11.0.1, 11.0.3, 11.0.4, 12.0.0, 12.1.0, 12.1.1, 12.0.3, 12.1.2, 12.0.4, 12.1.3, 13.0.0, 13.1.0. Software Version Numbers 9A, 9B…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0650-2023·2023-03-29

    DG Health Sugar Free Daily Fiber Recalled for Missing Phenylalanine Warning

    DG Health Sugar Free Daily Fiber is recalled for missing a required phenylalanine warning label. People with phenylketonuria (PKU) require this warning to safely use the product.

    Product
    DG Health brand Sugar Free Daily Fiber in 10 oz. plastic containers (UPC: 860005934294).
    Category
    Food
    Distribution
    47 states
  • HighNHTSA·23V211000·2023-03-29

    BMW seats may not restrain occupants properly in crash

    BMW is recalling certain 2019–2021 3-series and X3/X4 models because the seat frame may not have been welded properly to the seat rails, risking occupant injury in a crash.

    Product
    BMW — BMW X4, 330I, M340I, X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0639-2023·2023-03-29

    Japanese Potato Yokan Candy Recalled for Undeclared Coconut

    Kinjo Seika Potato Yokan confection is being recalled because coconut, a major allergen, was not declared on the label. Consumers with coconut allergies should not consume this product.

    Product
    Kinjo Seika Potato Yokan 130g UPC: 4901324017056 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1272-2023·2023-03-29

    Disposable Patient Circuit with Precision Flow System recalled for excessive condensation

    Vapotherm has recalled 5,869 Low Flow Disposable Patient Circuits for the Precision Flow System due to reports of excessive condensation that may lead to rainout.

    Product
    Low Flow Disposable Patient Circuit for the Precision Flow System, Product Code PF-DPC-LOW
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0473-2023·2023-03-29

    Daytrana Methylphenidate Transdermal Patches Recalled for Defective Delivery System

    Noven Pharmaceuticals recalls Daytrana (methylphenidate) 30 mg transdermal patches nationwide due to defective delivery system components that fail shear specifications. Patients should contact their healthcare provider regarding medication alternatives.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0627-2023·2023-03-29

    Alpha Rice Mushroom Rice Recalled for Undeclared Coconut Allergen

    Onishi Foods Alpha Rice Mushroom Rice is recalled due to undeclared coconut allergen on the label. Consumers with coconut allergies should not consume this product.

    Product
    Onishi Foods Alpha Rice Mushroom Rice 100g UPC: 4970088140546 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Drugs)·D-0471-2023·2023-03-29

    Daytrana Methylphenidate Patches Recalled for Defective Transdermal Delivery System

    Noven Pharmaceuticals is recalling specific lots of Daytrana (methylphenidate) transdermal patches due to a defective delivery system that is out of specification for shear. Affected lots are Lot 91956 (6/2023) and Lot 92475 (7/2023), distributed nationwide.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1266-2023·2023-03-29

    Attune Revision Tibial Insert Recalled for Excessive Gamma Radiation Exposure

    DePuy Orthopaedics is recalling 7 units of the Attune Revision Tibial Insert that received excess gamma radiation during manufacturing, which may degrade implant material properties.

    Product
    Attune Revision Limb Preservation System (LPS) Tibial Insert SM 12MM, Part Number 151760312
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0468-2023·2023-03-29

    Prescription Drug Recall: Jardiance Empagliflozin 25 mg Label Mix-Up

    Boehringer Ingelheim Pharmaceuticals is recalling Jardiance (Empagliflozin) 25 mg tablets due to a label mix-up affecting 69,375 bottles distributed nationwide.

    Product
    JARDIANCE — JARDIANCE (EMPAGLIFLOZIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1207-2023·2023-03-29

    BD Pyxis Automated Medication Dispensing Systems Firmware Downgrade Recall

    CareFusion recalls 7,914 units of BD Pyxis automated medication dispensing systems after firmware was inadvertently downgraded during installation, potentially causing drawer failures and medication delivery delays.

    Product
    BD Pyxis Anesthesia ES System (PAS ES), REF: 327; BP Pyxis MedStation ES (Med ES Main), REF: 323; BD Pyxis MedStation ES Tower (Med ES Tower), REF: 352; all with BD Pyxis ES version 1.6.1 drawer firmware (version 1.10.2.5). Pyxis MedStation Enterprise Server (ES) System is an…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0626-2023·2023-03-29

    MEITO Alphabet Chocolate recalled for undeclared coconut allergen

    MEITO Alphabet Chocolate 50g packages sold in multiple U.S. states and Canada were distributed with undeclared coconut allergen. Consumers with coconut allergies should not consume this product.

    Product
    MEITO Alphabet Chocolate 50g 50g UPC: 4902757130909 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighNHTSA·23V214000·2023-03-29

    2022 Volkswagen Taos Fuel Pump May Cause Engine Stall

    Volkswagen is recalling certain 2022 Taos vehicles because the fuel delivery pump may break and cause a sudden engine stall, increasing the risk of a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN TAOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1263-2023·2023-03-29

    Orthopedic Implant Recall: Excessive Radiation Exposure in Revision Tibial Insert

    DePuy Orthopaedics recalls 7 units of Attune Revision LPS Tibial Inserts (Part 151760118, Lot JP6452) distributed worldwide due to excessive gamma radiation during manufacturing. This overage may result in material property changes.

    Product
    Attune Revision Limb Preservation System (LPS) Tibial Insert XXSM 18MM, Part Number 151760118
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0644-2023·2023-03-29

    Onishi Foods Alpha Rice Recalled for Undeclared Coconut Allergen

    Onishi Foods Alpha Rice Matsutake Mushroom Rice is being recalled because the label does not declare coconut, a major allergen. The recall affects 733 units distributed in multiple US states and Canada.

    Product
    Onishi Foods Alpha Rice Matsutake Mushroom Rice 100g UPC: 4970088140331 Made in Japan
    Category
    Food
    Distribution
    6 states