The Recall Desk

State

Idaho product recalls

73,566 recalls have nationwide distribution and so reach Idaho. 3,523 additional recalls listed Idaho specifically in their distribution scope.

What the numbers show

Total
3,523
Critical
364
Severe
1,217
Most recent
2026-10-14

Of the 3,523 recalls naming Idaho we have scored against our rubric, 364 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,217 (35%) are Severe.

Which agencies issued them

These figures cover only the 3,523 recalls whose distribution notice names Idaho specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23726–23750 of 77089

  • ModerateFDA (Drugs)·D-0289-2022·2021-12-29

    Fexofenadine Hydrochloride Tablets 60 mg Recalled for Failed Impurities and Degradation Specifications

    The Harvard Drug Group is recalling Fexofenadine Hydrochloride Tablets, 60 mg, distributed by Major Pharmaceuticals nationwide due to failed impurities and degradation specifications. Affected lots are H00005, H00006, and H00007.

    Product
    Fexofenadine Hydrochloride Tablets, 60 mg, 500 Tablets per bottle, Distributed by: Major Pharmaceuticals, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152 NDC 0904-6979-40
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0404-2022·2021-12-29

    Stanbio TDM/B-Hydroxybutyrate Controls Recalled Due to Improper Storage Temperature

    Medline Industries is recalling Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls due to improper storage conditions. The product was shipped at room temperature instead of the required refrigerated environment.

    Product
    Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls, Ref. No. 2460-605
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateCPSC·22042·2021-12-29

    American Angler Electric Fillet Knives Recalled for Laceration Hazard

    Scott Fetzer Consumer Brands is recalling about 43,200 American Angler Electric Fillet Knives because the trigger mechanism can become stuck in the "on" position, posing a laceration hazard to users.

    Product
    American Angler Electric Fillet Knives
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V00M000·2021-12-28

    Hyundai recalls vehicles for windshield detachment risk in Santa Fe and other models

    Hyundai is recalling certain 2020-2021 Santa Fe, 2021 Sonata, and Elantra vehicles due to improper windshield bonding that may cause detachment during a crash. Dealers will reinstall windshields at no cost.

    Product
    HYUNDAI — HYUNDAI SANTA FE, SONATA, ELANTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V00K000·2021-12-28

    2022 Hyundai Santa Fe instrument cluster display may invert upon startup

    Hyundai is recalling certain 2022 Santa Fe PHEV and HEV vehicles because the instrument cluster display may invert upon startup, making it illegible and preventing drivers from seeing speed and safety warnings.

    Product
    HYUNDAI — HYUNDAI SANTA FE PLUG-IN HYBRID, SANTA FE HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V00J000·2021-12-27

    Mercedes-Benz Recalls 2022 EQS and S-Class for eCall Software Defect

    Mercedes-Benz is recalling 2022 EQS 450, S 500, and S 580 vehicles because a software defect may disable the emergency call system, potentially delaying emergency response.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQS 450, S 500 4MATIC, S 580 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22714·2021-12-23

    Polaris RZR and GENERAL Recreational Off-Road Vehicles Steering Wheel Separation Recall

    Polaris is recalling about 8,800 RZR and GENERAL recreational off-road vehicles because the steering wheel can separate, causing loss of control and crash risk. Polaris has received 33 reports of broken or cracked steering wheel spokes, including five rollovers and two injuries.

    Product
    Polaris RZR and GENERAL Recreational Off-Road Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E103000·2021-12-23

    Toyota power steering gear assembly recalled for oil leak risk

    Toyota is recalling power steering gear assemblies for certain Tundra and Sequoia models from 2007-2022. The components may be incorrectly manufactured, causing oil leaks that could result in sudden loss of power steering assist and increased crash risk.

    Product
    TOYOTA — TOYOTA SEQUOIA, TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V00H000·2021-12-23

    Freightliner Custom Chassis recreational vehicles electrical lighting system failure

    Daimler Trucks North America is recalling Freightliner Custom Chassis recreational vehicles with defective power distribution modules that may disable brake lights, turn signals, and rear marker lights, reducing visibility and increasing crash risk.

    Product
    FCCC — FCCC XBS, XBR, XBP, XCL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·22036·2021-12-22

    Angel Line Bunk Beds with Angled Ladders Recalled for Entrapment and Strangulation Risk

    Longwood Forest is recalling Angel Line bunk beds with angled ladders because the metal hook fastening the ladder can detach or move, creating gaps that pose serious entrapment and strangulation hazards. A 2-year-old child died in May 2018 when found unresponsive in a bunk bed ladder gap.

    Product
    Angel Line Bunk Beds with angled ladders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·22037·2021-12-22

    Royal Sovereign Portable Air Conditioners Recalled for Fire and Burn Hazards

    Royal Sovereign International is recalling about 33,570 portable air conditioners due to a faulty drain motor that can ignite the plastic enclosure, causing fires and burns. One death from smoke inhalation has been reported, along with 11 incidents of fires or smoking and over $1 million in property damage.

    Product
    Royal Sovereign/Royal Centurian portable air conditioners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·22040·2021-12-22

    Carex Adult Portable Bed Rails Recalled After Three Deaths

    Compass Health Brands is recalling Carex Brand Adult Portable Bed Rails due to entrapment and asphyxiation hazards. Three deaths have been reported when users became trapped within the rails or between the rail and mattress.

    Product
    Carex Brand Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·22039·2021-12-22

    Essential Medical Supply Endurance Hand Bed Rails Due to Entrapment and Asphyxiation

    Essential Medical Supply is recalling approximately 272,000 Endurance Hand Bed Rails because users can become entrapped within the rail or between the rail and mattress, posing a risk of asphyxiation. One death has been reported.

    Product
    Endurance® Hand Bed Rails
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0322-2022·2021-12-22

    Country Time Lemonade Drink Mix Powder Recalled for Glass and Metal Contamination

    Kraft Heinz Foods Company is recalling Country Time Lemonade drink mix powder in five sizes due to potential contamination with glass and metal fragments. The recall affects approximately 289,221 cases distributed nationwide and internationally.

    Product
    Country Time Lemonade drink mix powder 19 oz. UPC 043000951170 29 oz. UPC 043000951194 63 oz. UPC 043000082195 82.5 oz. UPC 043000928608 116 oz. UPC 043000075388
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V00F000·2021-12-22

    GM Recalls Buick and Chevrolet Vehicles for Rear Suspension Defect

    General Motors is recalling specific Buick and Chevrolet vehicles because rear suspension parts may corrode and fracture, increasing crash risk.

    Product
    BUICK — BUICK, CHEVROLET LACROSSE, REGAL, MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0280-2022·2021-12-22

    Lidocaine Topical Solution Recalled for Superpotency

    Teligent Pharma, Inc. is recalling Lidocaine Hydrochloride Topical Solution USP 4% nationwide due to the drug being superpotent. Affected lots are 13262 (Exp. 03/2022) and 14217 (Exp. 08/2022).

    Product
    Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL), 50 mL glass bottles, Rx Only, Teligent Pharma Inc., Buena, NJ 08310, NDC 52565-009-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0337-2022·2021-12-22

    FDA Class I Recall: Cardiosave Rescue Intra-Aortic Balloon Pump Fluid Ingress

    Datascope is recalling Cardiosave Rescue Intra-Aortic Balloon Pump devices due to possibility of fluid ingress, which could short electronic components and cause unsafe system shutdown.

    Product
    Cardiosave Rescue IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-75, 0998-UC-0800-75, 0998-00-0800-83, 0998-UC-0800-83, 0998-00-0800-85, 0998-UC-0800-85.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·22034·2021-12-22

    Hang-on Treestands Recalled Due to Cable Failure and Fall Hazard

    Big Game Treestands' 2021 The Captain model (batch 2M-0121) is recalled because plastic-coated cable crimps can slip during use, releasing the standing platform and causing falls. Two injuries have been reported from ten documented incidents.

    Product
    The Captain Hang-on Treestands (2021 Batch #2M-0121)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0336-2022·2021-12-22

    Cardiosave Hybrid IntraAortic Balloon Pump Recall Due to Fluid Ingress Risk

    Datascope Corp. is recalling Cardiosave Hybrid IntraAortic Balloon Pumps due to the risk of fluid entering the device, which could cause system failure and hemodynamic instability.

    Product
    Cardiosave Hybrid IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-UC-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-UC-0800-34, 0998-00-0800-35, 0998-UC-0800-35, 0998-00-0800-36, 0998-UC-0800-36, 0998-00-0800-45…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0375-2022·2021-12-22

    Cardinal Health Recalls RoyalSilk Surgical Gowns for Compromised Packaging Seals

    Cardinal Health is recalling 364,481 units of RoyalSilk Non-Reinforced Surgical Gowns due to potential for open packaging seals that could compromise sterility. The recalled units were distributed worldwide.

    Product
    RoyalSilk Non-Reinforced Surgical Gowns Large SKU: 9518
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0328-2022·2021-12-22

    Kool-Aid Ice Blue Raspberry Lemonade Drink Mix Recalled for Glass and Metal

    Kraft Heinz Foods Company is recalling Kool-Aid ice blue raspberry lemonade drink mix powder (20 oz.) due to potential glass and metal contamination in the product.

    Product
    Kool-Aid ice blue raspberry lemonade drink mix powder 20 oz. UPC 043000954072
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0365-2022·2021-12-22

    Orthopedic Femur Plate Recalled for Incorrect MRI Safety Information

    Smith & Nephew is recalling 35 units of EVOS Condylar Medial Distal Femur Plate due to incorrect MRI scanning safety information in the product instructions. The instructions contained erroneous data that could affect patient safety during MRI procedures.

    Product
    smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE, L, 5H, 115MM, REF 72573102
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0361-2022·2021-12-22

    Medline Venous Access Pack-LF Recalled for Expired Saline Component

    Medline is recalling Venous Access Pack-LF Convenience Kits because the included saline solution component expired before the kit's labeled expiration date, creating a quality and safety issue.

    Product
    Venous Access Pack-LF Convenience Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0330-2022·2021-12-22

    Kool-Aid Tropical Punch Drink Mix Recalled for Glass and Metal Contamination

    Kraft Heinz Foods is recalling Kool-Aid Tropical Punch "on the go" 10-pack drink mix powder due to potential contamination with glass and metal fragments. The affected product was distributed nationwide and internationally.

    Product
    Kool-Aid Tropical Punch "on the go" 10 pack net wt. 6.6 oz. drink mix powder UPC 043000023464
    Category
    Food
    Distribution
    Distributed nationwide