The Recall Desk

State

Utah product recalls

73,738 recalls have nationwide distribution and so reach Utah. 4,914 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total
4,914
Critical
524
Severe
1,350
Most recent
2026-10-28

Of the 4,914 recalls naming Utah we have scored against our rubric, 524 (11%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,350 (27%) are Severe.

Which agencies issued them

These figures cover only the 4,914 recalls whose distribution notice names Utah specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31576–31600 of 78652

  • HighFDA (Devices)·Z-1453-2020·2020-03-18

    Cardinal Health Recalls Non-Sterile Monoject Syringes with Safety Needles

    Cardinal Health is recalling Monoject 3mL syringes with safety needles because they were shipped as non-sterile despite labeling. The firm is not aware of any patient harm reports.

    Product
    Monoject 3mL Syringe with Hypodermic Safety Needle, 22G x 1-1/2 . Item Code 11832215 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampules and parts of the body below the surface of the skin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20725·2020-03-18

    Earth Sonnets Recalls Wintergreen Essential Oil for Packaging Defect

    Earth Sonnets is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.

    Product
    Earthsonnets Wintergreen (Gualtheria procumbens) Essential Oil
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V151000·2020-03-18

    Lamborghini Recalls 2020 Aventador SVJ Models for Door Handle Defect

    Lamborghini is recalling 26 2020 Aventador SVJ vehicles because the interior door handle mechanism may fail, preventing the door from opening from inside.

    Product
    LAMBORGHINI — LAMBORGHINI AVENTADOR SVJ COUPE, AVENTADOR SVJ ROADSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V156000·2020-03-18

    Mercedes-Benz and Freightliner Sprinter Recalled for Missing Spare Tire Label

    Daimler Vans USA is recalling 2018-2019 Sprinter vans because the spare tire may lack a maximum speed label, increasing the risk of tire failure.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 2500, SPRINTER 3500, SPRINTER 4500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1473-2020·2020-03-18

    Medicrea Iliac Screws Recalled Due to Incorrect Component Orientation

    Medicrea International is recalling 3,529 Iliac Screws because an internal component was assembled incorrectly, which may cause the tulip head to disengage from the shank.

    Product
    Iliac Screws, multiple sizes, Article Nos. B36020500 B36020570 B36020580 B36020590 B36027500 B36027570 B36027580 B36027590 B36028500 B36028570 B36028580 B36028590 B36029500 B36029570 B36029580 B36029590 Screws manufactured in titanium alloy Ti-6Al-4V LI…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1450-2020·2020-03-18

    Medtronic Simulus 850 Sizer Kits Recalled Due to Porcine Tissue Contact

    Medtronic is recalling six Simulus 850 Semi Rigid Ring/Band Accessory Kits because demonstration units may have contacted porcine tissue.

    Product
    Medtronic Simulus 850 Semi Rigid Ring/Band Accessory Kit Used to size a patient's mitral or tricuspid valve in cardiac procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1457-2020·2020-03-18

    EHOB Recalls Econocare Plus Waffle Overlay Due to Blood Contamination

    EHOB, Inc. is recalling specific lots of Econocare Plus Waffle Overlays due to potential contamination with human blood. No instances of contamination have been confirmed in distributed products.

    Product
    Econocare Plus Overlay Item: 1025EC. Intended to aid in the prevention and treatment of pressure injuries and general comfort - Product Usage: The EHOB WAFFLE Overlay intended use is as first line of defense for pressure injury prevention. The design provides the caregiver a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20091·2020-03-18

    Novartis Recalls 100 mg Sandimmune and Neoral Blister Packages for Packaging Defect

    Novartis is recalling 100 mg Sandimmune and Neoral blister packages because they fail child-resistant packaging requirements, posing a poisoning risk to children.

    Product
    Sandimmune® (cyclosporine capsules, USP) 100 mg soft gelatin capsules and Neoral® (cyclosporine capsules, USP) MODIFIED 100 mg soft gelatin capsules prescription drug blister packages
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1472-2020·2020-03-18

    Medicrea Recalls Pedicle Screws Due to Incorrect Component Orientation

    Medicrea International is recalling 3,529 pedicle screws because an internal component was assembled incorrectly, which may cause the tulip head to disengage from the screw shank.

    Product
    Pedicle Screws, multiple sizes, Article Nos. B36004525 B36004530 B36004535 B36004540 B36004545 B36004550 B36004555 B36005530 B36005535 B36005540 B36005545 B36005550 B36005555 B36005560 B36006530 B36006535 B36006540 B36006545 B36006550 B36006555 B36006560…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20093·2020-03-18

    Belle Chemical Recalls Sodium and Potassium Hydroxide for Packaging Defects

    Belle Chemical is recalling sodium and potassium hydroxide products because they lack required child-resistant packaging and proper hazard labeling.

    Product
    Sodium Hydroxide, Lye/Caustic Soda and Potassium Hydroxide, Caustic Potash Ash
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V152000·2020-03-18

    BMW Recalls X3 and X4 Models for Instrument Panel Casing Defect

    BMW is recalling 2018-2020 X3 and 2019-2020 X4 vehicles because the instrument panel casing may not be tightened properly, posing an injury risk during air bag deployment.

    Product
    BMW — BMW X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1454-2020·2020-03-18

    Cardinal Health Recalls Non-Sterile Monoject Hypodermic Safety Needles

    Cardinal Health is recalling Monoject Hypodermic Safety Needles because they were shipped as non-sterile despite labeling indicating sterility, posing an infection risk.

    Product
    Monoject Hypodermic Safety Needle 30G X 1/2" Item Code 1183005 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampules and parts of the body below the surface of the skin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1456-2020·2020-03-18

    Cardinal Health Recalls Non-Sterile Monoject Bluntfill Syringes

    Cardinal Health 200, LLC is recalling Monoject Bluntfill syringes that were shipped as non-sterile but labeled as sterile. The firm is not aware of any patient harm.

    Product
    Monoject Bluntfill with Filter, 18G x 1-1/2" Item Code 11811022F. Used for drawing fluid from a vial - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampules and parts of the body below the surface of the skin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1449-2020·2020-03-18

    Medtronic Simulus 750 Flexible Ring/Band Accessory Kit Recalled for Tissue Contact

    Medtronic CoreValve LLC is recalling six Simulus 750 Flexible Ring/Band Accessory Kits because demonstration units may have contacted non-human tissue.

    Product
    Medtronic Simulus 750 Flexible Ring/Band Accessory Kit - Product Usage: Used to size a patient's mitral or tricuspid valve in cardiac procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20092·2020-03-18

    Boyer Recalls Six Brands of Sodium and Potassium Hydroxide for Packaging Defects

    The Boyer Corporation is recalling six brands of sodium and potassium hydroxide products because the packaging is not child-resistant, posing a risk of chemical burns.

    Product
    Soap Supply Co. Lye, Soap Makers Lye, California Soap Supply, Combo Pure Solutions, Red Crown High Test Lye, and Boyer Potassium Hydroxide Flakes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1056-2020·2020-03-18

    Lupin Recalls Levonorgestrel and Ethinyl Estradiol Tablets for Content Uniformity

    Lupin Pharmaceuticals is recalling specific lots of oral contraceptive tablets due to failed content uniformity tests.

    Product
    Levonorgestrel and Ethinyl Estradiol Tablets USP, 0.05mg/0.03 mg, 0.075mg/0.04mg, and 0.125mg/0.03mg, packaged in 1 Wallet of 28 Tablets (NDC 68180-857-11), 3 Wallets of 28 Tablets Each per carton (NDC 68180-857-13); Rx Only, Distributed by: Lupin Pharmaceuticals, Inc.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1471-2020·2020-03-18

    Verathon Recalls GlideScope Video Laryngoscope Operations and Maintenance Manuals

    Verathon, Inc. is recalling 239 GlideScope Video Laryngoscope Operations & Maintenance Manuals due to a typographical error regarding disinfection instructions.

    Product
    GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03
    Category
    Medical Device
    Distribution
    33 states
  • ModerateFDA (Devices)·Z-1461-2020·2020-03-18

    Response Biomedical Recalls RAMP Cardiac Controls Due to Signal Loss

    Response Biomedical Corp. is recalling RAMP Cardiac Controls because CK-MB levels decreased by up to 57% within 11 months, potentially affecting quality control results.

    Product
    Randox Laboratories Ltd. Catalogue Number CQ5052, Lot Number 4244CK (relabeled as Response Biomedical Catalogue Number C2003-2, Lot #070318) IFU: "RAMP Cardiac Controls *** CAT. No.: C2003-2 *** Size: 3 x 3 ML". Product Usage: use in the quality control of cardiac…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1460-2020·2020-03-18

    Braemar DL950 Holter Monitor Recall Due to Startup Error

    Braemar Manufacturing is recalling DL950 Holter Monitors because a software issue prevents new patient studies from starting.

    Product
    Braemar Manufacturing LLC DL950 Holter Monitor 1285 Corporate Center Dr. Suite 150 Eagan, MN 55121 USA Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0826-2020·2020-03-18

    Siete Grain Free Tortillas Recalled for Sodium Labeling Error

    Garza Food Ventures is recalling Siete Grain Free Burrito Size Tortillas because the sodium content is 340 mg per serving, not the 15 mg declared on the label.

    Product
    Siete Grain Free Burrito Size Tortillas Net Wt 15 oz (423g) 6 count UPC 865336000083 packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateCPSC·20094·2020-03-18

    Belle Chemical Recalls Drain Cleaner for Missing Poison Labeling

    Belle Chemical is recalling 100% Sodium Hydroxide Drain Cleaner because the label violates the Federal Hazardous Substance Act by omitting the word 'poison' and mandatory hazard statements.

    Product
    100% Sodium Hydroxide Drain Cleaner
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0998-2020·2020-03-18

    Mayne Pharma Recalls Carbidopa and Levodopa Tablets Due to Foreign Tablet Mix-Up

    Mayne Pharma is recalling specific bottles of Carbidopa and Levodopa Tablets because a foreign tablet was found in a bottle.

    Product
    Carbidopa and Levodopa Tablets, USP 25 mg/250mg, 100 ct bottle, Rx Only, Mayne Pharma, Greenville, NC 27834. NDC 51862-858-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1459-2020·2020-03-18

    Braemar DL900 Holter Monitor Recalled for Operational Failure

    Braemar Manufacturing is recalling DL900 Holter Monitors because a software issue prevents new patient studies from starting. Existing recordings can still be downloaded.

    Product
    Braemar Manufacturing LLC DL900 Holter Monitor 1285 Corporate Center Dr. Suite 150 Eagan, MN 55121 USA Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide