The Recall Desk

State

Idaho product recalls

73,096 recalls have nationwide distribution and so reach Idaho. 3,520 additional recalls listed Idaho specifically in their distribution scope.

What the numbers show

Total
3,520
Critical
364
Severe
1,025
Most recent
2026-09-23

Of the 3,520 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 1,025 (29%) are Severe.

These figures cover only the 3,520 recalls whose distribution notice names Idaho specifically. The 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8426–8450 of 76616

  • SevereNHTSA·25V015000·2025-01-16

    GM electric pickup rear centre seat belt bolt may be loose

    General Motors is recalling certain 2024 Chevrolet Silverado EV and 2024-2025 GMC Sierra EV pickups because the bolt securing the rear centre seat belt to the seat structure may not be properly tightened.

    Product
    GMC — GMC, CHEVROLET SIERRA EV, SILVERADO EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V016000·2025-01-16

    Land Rover touchscreen can go blank hiding the rearview camera image

    Land Rover is recalling certain 2023 Discovery Sport, 2023-2024 Defender and 2023 Range Rover Evoque vehicles because the centre console touchscreen may go blank at startup, failing FMVSS 111.

    Product
    LAND ROVER — LAND ROVER DEFENDER, DISCOVERY SPORT, RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V012000·2025-01-16

    Chevrolet Equinox EV adaptive cruise control may not brake as expected

    General Motors is recalling certain 2025 Chevrolet Equinox EV all-wheel drive vehicles because incorrect brake module software may stop adaptive cruise control engaging the brakes as expected.

    Product
    CHEVROLET — CHEVROLET EQUINOX EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25094·2025-01-16

    HallyBee Farmhouse Dressers Recalled for Tip-Over and Entrapment Hazards

    About 122 HallyBee Farmhouse 5-Drawer Dressers sold on Amazon from September 2023 to October 2024 are recalled due to tip-over and entrapment hazards when not anchored to a wall, risking injury or death to children.

    Product
    HallyBee Farmhouse 5-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25090·2025-01-16

    Lexmark Specialty Printers Recalled Due to Fire Hazard

    Lexmark is recalling about 43,510 MS725dvn and MX725adve specialty printers because a metal part can dislodge and cause fire. One fire has been reported, though no injuries or damage resulted.

    Product
    MS725dvn and MX725adve Specialty Printers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25092·2025-01-16

    Polaris Ranger XD and Crew XD Recreational Vehicles Recalled for Door Latch Failure

    Polaris is recalling about 4,200 Ranger XD and Crew XD recreational off-road vehicles because door handles can stick, causing doors to unexpectedly open while the vehicle is moving. This poses a risk of occupant ejection and crashes.

    Product
    Model Year 2024-2025 Ranger XD 1500 and Crew XD 1500 ROVs
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0712-2025·2025-01-15

    Vasoview Hemopro 2 Vessel Harvesting System Recalled for Heater Wire and Silicone Defects

    Maquet Cardiovascular is recalling the Vasoview Hemopro 2 Vessel Harvesting System due to potential heater wire and silicone defects. These could affect device function during minimally invasive surgery.

    Product
    Vasoview Hemopro 2 (w/Vasoshield) Endoscopic Vessel Harvesting System. Model Numbers: VH-4001. Indicated for use in minimally invasive surgery allowing access for vessel harvesting.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0711-2025·2025-01-15

    VasoView HemoPro 2 Endoscopic Vessel Harvesting System Class I Recall

    FDA recalls VasoView HemoPro 2 endoscopic vessel harvesting systems due to risk of heater wire detachment and silicone peeling from the harvesting tool jaws, which could affect device function.

    Product
    VasoView HemoPro 2 Endoscopic Vessel Harvesting System. Model Numbers: VH-4000. Indicated for use in minimally invasive surgery allowing access for vessel harvesting.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0763-2025·2025-01-15

    Large Volume Pump model LVP-0004 recalled for potential pneumatic valve failure

    Fresenius Kabi is recalling 1,520 Ivenix infusion pumps (model LVP-0004) due to potential pneumatic valve failure that may stop active infusions or prevent pump operation. Affected units were distributed to healthcare facilities in six U.S. states.

    Product
    Ivenix Infusion System (IIS), Large Volume Pump, Model Number: LVP-0004
    Category
    Medical Device
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0181-2025·2025-01-15

    Clonazepam Tablets Recalled Due to Carton Labeling Error

    Endo USA, Inc. is recalling 22,513 cartons of clonazepam tablets due to incorrect strength labeling on some carton exteriors. The actual tablets inside have correct labeling.

    Product
    CLONAZEPAM — CLONAZEPAM (CLONAZEPAM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0378-2025·2025-01-15

    Greek yogurt tzatziki products recalled for potential salmonella

    US Foods Chef's Line and Nick The Greek tzatziki products distributed across multiple states are being recalled due to potential salmonella contamination. Consumers should not consume these products.

    Product
    US Foods Chef's Line Greek Yogurt Tzatziki 4lbs tub, UPC 758108679962, SKU SAL519448, 2 tubs per case. Nick The Greek Tzatziki Pail, 42lbs pail, UPC 10075365177787, SKU SA000084
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Drugs)·D-0177-2025·2025-01-15

    Herbal Capsules Recalled Nationwide for Undeclared Pharmaceutical Ingredients

    Herbal capsules sold nationwide have been recalled after the FDA found undeclared medications inside. The product contained furosemide, dexamethasone, and chlorpheniramine without proper labeling.

    Product
    Nhan Sam Tuyet Lien Truy Phong Hoan, Capsules, 30-Count Bottles, Manufactured by Yee Hong Pharmaceuticals, SDN, Penang, Malasia.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0180-2025·2025-01-15

    Clonazepam Tablets Recalled Due to Incorrect Carton Labeling

    Endo USA recalls clonazepam tablets because some cartons are labeled with incorrect declared strength. The medication inside the blister strips contains the correct strength.

    Product
    CLONAZEPAM — CLONAZEPAM (CLONAZEPAM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0379-2025·2025-01-15

    Spicy Yogurt Pails Recalled for Potential Salmonella Contamination

    Grecian Delight/Kronos is recalling Nick The Greek Spicy Yogurt Pails (Lot 4305) due to potential salmonella contamination. The 42-lb pails were distributed across 27 U.S. states.

    Product
    Nick The Greek Spicy Yogurt Pail, 42lbs pail, UPC 10075365177756, SKU SA000085
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Drugs)·D-0178-2025·2025-01-15

    Clonazepam tablets recalled for incorrect carton labeling

    Endo USA is recalling approximately 9,816 cartons of Clonazepam 2 mg tablets due to incorrect strength labeling on the carton exterior. The blister strips inside contain the correct formulation.

    Product
    CLONAZEPAM — CLONAZEPAM (CLONAZEPAM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0377-2025·2025-01-15

    Grecian Delight and Sysco Classic Tzatziki Sauce Recalled for Potential Salmonella

    Grecian Delight and Sysco Classic tzatziki sauce may contain Salmonella. Consumers should discard the product or return it to their retailer.

    Product
    Grecian Delight Tzatziki sauce, 3.75 lb. tub, UPC 07365000286, SKU SAL028, 4 tubs per case. Sysco Classic Tzatziki sauce, 3.75 lb. tub, UPC 074865886277, SKU SAL9669136, 4 tubs per case.
    Category
    Food
    Distribution
    27 states
  • HighFDA (Drugs)·D-0191-2025·2025-01-15

    FDA Recalls Radiopharmaceutical Kit Due to Failed Stability Specifications

    Jubilant Draximage is recalling 5,209 kits of Technetium Tc 99m Sulfur Colloid Injection that failed stability specifications. The affected lots (C2300070, C2300070E) were distributed nationwide.

    Product
    Kit for the Preparation of Technetium Tc 99m Sulfur Colloid Injection, 10 mL Multi-Dose Reaction Vial, 5 vial Box, Rx Only, Manufactured for: Jubilant Draximage Inc., dba Jubilant Radiopharma, Kirkland , Quebec, H9H, 4J$, Canada, NDC# 65174-179-05.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0187-2025·2025-01-15

    Colchicine Capsules Recalled Due to Failed Dissolution Specifications

    Granules Pharmaceuticals is recalling Colchicine 0.6 mg capsules nationwide due to failed dissolution specifications detected during stability testing. Patients should contact their healthcare provider for guidance.

    Product
    COLCHICINE — COLCHICINE (COLCHICINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0809-2025·2025-01-15

    Xhibit Telemetry Receiver may shut down, causing temporary loss of patient monitoring

    Spacelabs Healthcare's Xhibit Telemetry Receiver (Model 96280) may experience a Windows proxy issue causing the system to restart and go offline for 1-1.5 minutes, creating a temporary gap in patient monitoring.

    Product
    Xhibit Telemetry Receiver, Model 96280, with Service Manual. Intended to provide monitoring system with patient data.
    Category
    Medical Device
    Distribution
    44 states