The Recall Desk

State

Idaho product recalls

73,495 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 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21851–21875 of 77018

  • HighFDA (Devices)·Z-1020-2022·2022-05-11

    Estradiol diagnostic test kits recalled for falsely elevated results

    Siemens Atellica IM Enhanced Estradiol test kits can produce falsely elevated results in plasma specimens, potentially leading to misinterpretation of patient hormone measurements. Approximately 2,044 units worldwide are affected.

    Product
    Atellica IM Enhanced Estradiol (eE2) 100T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10995561 All lots
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1025-2022·2022-05-11

    Estradiol Diagnostic Device Recalled for Falsely Elevated Test Results

    An estradiol diagnostic device has been recalled because it produces falsely elevated test results in plasma specimens. These inaccurate results could cause clinicians to misinterpret patient test results.

    Product
    ADVIA Centaur Enhanced Estradiol (eE2) (REF) 500T - In vitro diagnostic use in the quantitative detection of estradiol SMN: 10697757 All lots
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0834-2022·2022-05-11

    Losartan Potassium Tablets Recalled for Excessive Azido Impurity

    Macleods Pharma is recalling Losartan Potassium Tablets due to CGMP deviations with azido impurity levels exceeding acceptable limits. The recall affects 5.6 million tablets distributed nationwide.

    Product
    LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0831-2022·2022-05-11

    Drug recall: Vancomycin HCl injection bags for manufacturing deviations

    SCA Pharmaceuticals has recalled Vancomycin HCl 1.5g injection bags due to manufacturing process deviations. The product was distributed nationwide.

    Product
    Vancomycin HCl 1.5 g in 0.9% Sodium Chloride, 500 mL bags, Rx only, SCA Pharmaceuticals Windsor, CT 06095, NDC 70004-0924-44
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0851-2022·2022-05-11

    Erythromycin Topical Gel Recalled Due to Manufacturing Quality Deviations

    McKesson Corporation is recalling Erythromycin Topical Gel USP 2% due to CGMP deviations. The manufacturer discontinued its stability study program, prompting a nationwide recall of all products within their expiration date.

    Product
    Erythromycin Topical Gel USP, 2%, Net Wt 60 g tube, Rx only, Manufactured by: Teligent Pharma, Inc. Buena, NJ 08310 Distributed by: McKesson Corporation dba Sky Packaging 4971 Southridge Blvd., Suite 101 Memphis, TN 38141, NDC 63739-053-68
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0846-2022·2022-05-11

    Lidocaine Oral Topical Solution Recalled Due to Failed Viscosity Specification

    Akorn, Inc. is recalling 66,744 bottles of Lidocaine Hydrochloride Oral Topical Solution, USP 2% (Lot #370978) nationwide because the product's viscosity was below the required specification.

    Product
    Lidocaine Hydrochloride Oral Topical Solution, USP (Viscous) 2%, 100 mL per bottle, Rx only, Manufactured by Hi-Tech Pharmacal Co., Inc. Amityville, NY 11701, NDC 50383-775-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1026-2022·2022-05-11

    Cervical Cage Trial Kit Recalled for Incorrect Size Labeling

    restor3d Inc. is recalling 14 units of its Non-Sterile Double Ended Trial Kit because the product was labeled as Small Footprint when it is actually Medium. The lot was distributed nationwide across seven states.

    Product
    Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the Cervical Cage. The kit includes 3 trials. Orthopedic manual surgical instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0829-2022·2022-05-11

    Norepinephrine Injection Recalled Nationwide for Manufacturing Quality Deviations

    SCA Pharmaceuticals recalled 120 bags of Norepinephrine 8mg injection nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The voluntary recall was initiated April 25, 2022.

    Product
    Norepinephrine 8mg in 0.9% Sodium Chloride 250 mL bag, Rx only, SCA Pharmaceuticals Windsor, CT 06095, NDC 70004-078-40
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0842-2022·2022-05-11

    Losartan Potassium and Hydrochlorothiazide Tablets Recalled for Impurity

    Lupin Pharmaceuticals is recalling Losartan Potassium and Hydrochlorothiazide 100 mg/25 mg tablets nationwide due to AZIDO impurity levels above acceptable limits. Patients should consult their healthcare provider about their medication.

    Product
    LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0837-2022·2022-05-11

    Losartan Potassium and Hydrochlorothiazide Tablets Recalled Due to AZIDO Impurity Contamination

    Macleods Pharma USA is recalling Losartan Potassium and Hydrochlorothiazide tablets due to AZIDO impurity levels exceeding acceptable manufacturing standards. The prescription blood pressure medication was distributed nationwide.

    Product
    LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0830-2022·2022-05-11

    Drug recall: fentanyl and bupivacaine injectable solution manufacturing deviations

    SCA Pharmaceuticals voluntarily recalled 424 bags of fentanyl and bupivacaine injectable solution due to manufacturing control deviations. The product was distributed nationwide in the United States.

    Product
    Fentanyl 2mcg/ml and Bupivacaine 0.125% in 0.9% Sodium Chloride 100 mL bags, Rx only, SCA Pharmaceuticals Windsor, CT 06095, NDC 70004-0231-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V320000·2022-05-10

    Land Rover Recalls 2022 New Range Rovers for Front Crash Sensor Defect

    Jaguar Land Rover is recalling 2022 New Range Rovers because improperly tightened fasteners may cause front crash sensors to malfunction, affecting air bag deployment.

    Product
    LAND ROVER — LAND ROVER NEW RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V318000·2022-05-10

    Braxton Creek Recalls 2022 Travel Trailers Due to LP Gas Leak Risk

    Braxton Creek RV is recalling 2022 Free Solo, Bushwhacker, and Bushwhacker Plus travel trailers because cracked LP gas fittings may cause a leak and fire.

    Product
    BRAXTON CREEK — BRAXTON CREEK BUSHWACKER, BUSHWACKER PLUS, FREE SOLO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V319000·2022-05-10

    2022 Rivian R1T front passenger seat airbag may not deactivate for children

    Certain 2022 Rivian R1T vehicles have a malfunctioning occupant classification system that fails to deactivate the front passenger airbag when a child or child seat is present, increasing injury risk during a crash.

    Product
    RIVIAN — RIVIAN R1T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V313000·2022-05-09

    2023 Winnebago Ekko RV Recalled for Cracked LP Gas Fittings

    Winnebago is recalling 2021-2023 Ekko recreational vehicles because quick disconnect fittings in the LP gas system may crack, potentially causing a gas leak that could lead to fire.

    Product
    WINNEBAGO — WINNEBAGO EKKO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V316000·2022-05-09

    Custom Fire Recalls Spartan Emergency Vehicles Due to Axle Defect

    Custom Fire is recalling 2021-2022 Spartan emergency vehicles because a rear axle part may fracture, potentially causing the parking brake to engage unexpectedly and increasing crash risk.

    Product
    CUSTOM FIRE — CUSTOM FIRE SPARTAN METROSTAR, SPARTAN METROSTAR RT, SPARTAN GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V315000·2022-05-09

    Mercedes-Benz Recalls Vehicles Due to Brake Booster Corrosion Risk

    Mercedes-Benz is recalling 2006-2012 ML, GL, and R-Class vehicles because moisture in the brake booster can cause corrosion, leading to reduced brake performance or failure.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ R350, ML350, AMG ML63, GL320
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V314000·2022-05-09

    Mercedes-Benz Recalls 2021 GLB 250 for Rear Axle Sensor Defect

    Mercedes-Benz is recalling 2021 GLB 250 vehicles because a rear axle sensor linkage may be improperly installed, potentially causing headlight glare that increases crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V317000·2022-05-09

    2020-2021 Tesla Model 3: Swapped Camera Terminals Impair Collision Detection

    Tesla recalls 2020-2021 Model 3 and 2021 Model Y vehicles due to incorrectly installed camera cable terminals that cause swapped camera views, impairing collision detection and automatic emergency braking.

    Product
    TESLA — TESLA MODEL Y, MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22T007000·2022-05-06

    Sumitomo and Falken Tires Recalled for Bead Separation Risk

    Sumitomo is recalling certain Sumitomo and Falken tires because a deformation near the bead could cause separation, increasing the risk of a crash.

    Product
    TIRES:BEAD recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V311000·2022-05-06

    Hyundai Accent vehicles recalled for unsecured steering column bolt

    Hyundai is recalling 2021-2022 Accent vehicles because a steering column bolt may not be properly secured. This can cause the steering column to detach, resulting in loss of steering control and increased crash risk.

    Product
    HYUNDAI — HYUNDAI ACCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide