The Recall Desk

State

Idaho product recalls

20,199 recalls have nationwide distribution and so reach Idaho. 0 additional recalls listed Idaho specifically in their distribution scope.

About recalls in Idaho

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Idaho consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

10926–10950 of 20199

  • HighCPSC·24041·2023-12-07

    Nap Queen Maxima Hybrid Mattresses Recalled for Fire Hazard

    Adven Group LLC is recalling about 1,540 Nap Queen 12-inch Maxima Hybrid Mattresses sold via Amazon, Walmart, and Overstock because they fail to meet federal flammability standards and pose a fire hazard.

    Product
    Nap Queen 12-inch Maxima Hybrid Mattress
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24731·2023-12-07

    Moonsea Pack and Play Mattresses Recalled for Suffocation Hazard

    Moonsea Pack and Play Mattresses sold on Amazon violate federal crib mattress safety regulations and pose a suffocation hazard to infants. Consumers should stop using them immediately and contact Moonseasleep for a refund.

    Product
    Moonsea Pack and Play Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24040·2023-12-07

    SABRE Aim & Fire Pepper Gel Spray Canisters Failure to Deploy

    Security Equipment Corporation is recalling about 4,000 SABRE Aim & Fire Pepper Gel Spray canisters with expiration date 9/2027 because they lack a red nozzle needed to deploy the spray and will not function in an emergency. No injuries have been reported.

    Product
    SABRE Aim & Fire Pepper Gel Spray with Training Canisters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24042·2023-12-07

    Mary Meyer Bubba Bull Plush Toys Recalled for Choking Hazard

    Mary Meyer is recalling about 1,950 Bubba Bull Plush Toys because the eyes can break off and pose a choking hazard to young children. No injuries have been reported.

    Product
    Bubba Bull Plush Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V477000·2023-12-07

    Jayco Seneca recreational vehicles recalled for windshield wiper linkage failure

    Jayco is recalling certain 2021-2022 Seneca recreational vehicles because the windshield wiper arms may fail, reducing driver visibility and increasing crash risk. Owners should contact Jayco customer service at 1-800-283-8267 for a free inspection and replacement.

    Product
    JAYCO — 2021 JAYCO SENECA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V478000·2023-12-07

    2021-2022 Toyota RAV4 Prime recalled for electrical fire risk

    Toyota is recalling 43,442 2021-2022 RAV4 Prime and 2022 Lexus NX450H+ plug-in hybrid vehicles. A defective DC-DC converter electrical module can overheat and cause vehicle fire. Dealers will replace the component free of charge.

    Product
    TOYOTA — 2021 TOYOTA RAV4 PRIME
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24047·2023-12-07

    Windsor Queen Xtrabed Mobile Murphy Beds Recalled for Injury and Tip-Over Hazards

    SourceOne Ventures recalls Windsor Queen Xtrabed Mobile Murphy Beds due to risks of cabinet breakage and tip-over. About 12,000 units sold at Wayfair between November 2016 and April 2023 are affected.

    Product
    Windsor Queen Xtrabed Mobile Murphy Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V476000·2023-12-07

    Polestar 2 Recalled for Potential Steering Loss Due to Defective Ball Joint

    Polestar is recalling certain 2023 Polestar 2 vehicles due to a defect in the front left lower ball joint that could cause loss of steering control. Owners should contact their dealer for a free inspection and replacement.

    Product
    POLESTAR — 2023 POLESTAR POLESTAR 2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·24733·2023-12-07

    Bunkhouse and Lotsa LITES! Mini String Lights Recalled for Burn and Fire Hazards

    Bunkhouse and Lotsa LITES! Connectable Mini String Lights can overheat and present burn and fire hazards when plugged directly into an outlet. About 34,600 units are affected.

    Product
    Bunkhouse and Lotsa LITES! Connectable Mini String Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24728·2023-12-07

    Ergodyne Squids 3705 Wire Tool Attachments Recalled for Injury Hazard

    Ergodyne is recalling about 16,570 Squids 3705 Wire Tool Attachments because the wire can break when dropped while tethering a tool over two pounds, posing an injury risk to bystanders below.

    Product
    Squids 3705 Wire Tool Attachments - Screw Gate Tool Tail
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24730·2023-12-07

    Bugaboo Dragonfly Seat Strollers Recalled for Infant Fall Injury Hazard

    Bugaboo is recalling about 1,000 Dragonfly Seat Strollers because the backrest can move downward in parent-facing mode, causing unrestrained infants to potentially tumble from the seat. No U.S. injuries have been reported.

    Product
    Bugaboo Dragonfly Seat Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24039·2023-12-07

    Oreck Discover Upright Vacuums Recalled Due to Electrical Shock Hazard

    The electric cord plug prong on Oreck Discover Upright Vacuums can detach and remain in electrical outlets, creating an electrical shock hazard. About 6,200 units sold nationwide from September 2022 through September 2023 are affected.

    Product
    Oreck Discover Upright Vacuums
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0226-2024·2023-12-06

    Kuka Flex Forte caplets recalled for undeclared diclofenac and lack of FDA approval

    Botanical Be is recalling Kuka Flex Forte caplets nationwide because they contain undeclared diclofenac and were marketed without required FDA approval. All lots expire 12/12/2024.

    Product
    Kuka Flex Forte caplets, packaged in 30-count bottles, Manufactured by: Kukamonga, Gonzalez Ortega No 170 Col Centro, 44100 Guadalajara Jal, UPC 0736640810265
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V421000·2023-12-06

    2022 Nissan Sentra: Driver Cowl Seal Defect May Cause Electrical Failures

    The 2022 Nissan Sentra may have a defective driver's side cowl seal, allowing water intrusion and electrical corrosion. This could cause loss of airbag function, exterior lighting, and braking safety features, increasing crash and fire risk.

    Product
    NISSAN — 2022 NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0224-2024·2023-12-06

    FDA recalls Artri King tablets for undeclared diclofenac

    Botanical Be is recalling 235 bottles of Artri King tablets sold nationwide. The tablets contain undeclared diclofenac and were marketed without FDA drug approval.

    Product
    Artri King Reforzado con Origa y Omega 3 tablets, packaged in 100-count bottles, Manufactured by: Plantas medicinales de Mexico, Melchol Ocampo # 65 Local D, Delegacion Xochimilco CP 16800, Mexico DF, UPC 7 501031 111138
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0225-2024·2023-12-06

    Reumo Flex caplets recalled for undeclared diclofenac content nationwide

    Reumo Flex caplets packaged in 30-count boxes are being recalled because they contain undeclared diclofenac and were marketed without FDA approval. The product was distributed nationwide.

    Product
    Reumo Flex caplets, packaged in 30-count boxes, Manufactured by: Grupo Yepenza de Mexico, SA de CV, Comerciantes 5824 Col Arcos de Guadalupe, Zapopan Jal Mexico, UPC 7 502214 014598
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0145-2024·2023-12-06

    Prescription drug oral solution recalled for microbial contamination

    Bayer Healthcare Pharmaceuticals Inc. is recalling 192 bottles of VITRAKVI (larotrectinib) oral solution due to microbial contamination identified as Penicillium brevicompactum during routine testing.

    Product
    VITRAKVI — VITRAKVI (LAROTRECTINIB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V455000·2023-12-06

    2022 Lincoln Navigator Headlight Control Software Defect Causes Light Failure

    Ford is recalling certain 2022 Lincoln Navigator vehicles due to headlight control module software that may fail, causing side marker and daytime running lights to go dark. This increases crash risk from reduced visibility.

    Product
    LINCOLN — 2022 LINCOLN NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0123-2024·2023-12-06

    Prescription Drug Indomethacin Recalled Due to Label Mix-Up

    Glenmark Pharmaceuticals is recalling 37,200 bottles of Indomethacin 25mg capsules distributed nationwide because the bottles may be labeled as Naproxen instead. This labeling error could cause medication confusion.

    Product
    INDOMETHACIN — INDOMETHACIN (INDOMETHACIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V454000·2023-12-06

    2022 Lincoln Aviator Engine Rails Defect Increases Crash Injury Risk

    Ford is recalling certain 2022 Lincoln Aviator vehicles due to improperly heat-treated engine rails that may reduce structural protection in crashes and potentially detach while driving. Owners should contact Ford for a free inspection and replacement.

    Product
    LINCOLN — 2022 LINCOLN AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0422-2024·2023-12-06

    RAPIDPOINT 500e Blood Gas System Recalled Due to Drug Interference

    Siemens RAPIDPOINT 500e blood gas systems may show falsely elevated sodium readings in patients taking Perhexiline Maleate or Atomoxetine, risking misdiagnosis and inappropriate treatment of electrolyte imbalances.

    Product
    RAPIDPOINT 500e Blood Gas System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V450000·2023-12-06

    2022 Forest River R-POD Trailers Recalled for Incorrect Axle Rating

    Forest River is recalling 205 2022 R-POD travel trailers because the Federal Placard shows an incorrect axle rating (4400 lbs instead of 3500 lbs), which can cause overload and loss of control.

    Product
    FOREST RIVER — 2022 FOREST RIVER R-POD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0423-2024·2023-12-06

    RAPIDPOINT 500 Blood Gas System: Drug Interference May Cause False Sodium Readings

    Siemens RAPIDPOINT 500 Blood Gas System may produce falsely elevated sodium results due to drug interference from Perhexiline Maleate or Atomoxetine Hydrochloride. This could lead to missed hyponatremia or inappropriate treatment of hypernatremia.

    Product
    RAPIDPOINT 500 Blood Gas System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0121-2024·2023-12-06

    Paroxetine Hydrochloride 30 mg Tablets Recalled for Impurity Specification Failure

    Apotex Corp. is recalling nationwide 25,776 units of Paroxetine Hydrochloride 30 mg tablets due to out-of-specification impurities. Affected lot numbers RV8686, RX0119, and RV2254 expire 08/2024.

    Product
    PAROXETINE — PAROXETINE (PAROXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0122-2024·2023-12-06

    Paroxetine Hydrochloride Tablets Recalled for Out-of-Specification Impurity

    Apotex Corp. is recalling Paroxetine Hydrochloride 40 mg tablets nationwide due to failed quality specifications. Testing found out-of-specification impurity levels in affected lot numbers.

    Product
    PAROXETINE — PAROXETINE (PAROXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide