The Recall Desk

State

Utah product recalls

20,322 recalls have nationwide distribution and so reach Utah. 0 additional recalls listed Utah specifically in their distribution scope.

About recalls in Utah

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 Utah 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.

13076–13100 of 20322

  • HighNHTSA·22V263000·2023-06-04

    Tesla Model 3 Speedometer Unit Display May Fail in Track Mode

    Tesla is recalling certain 2018-2022 Model 3 Performance vehicles because the speedometer's mph/km/h unit display may fail in Track Mode. Drivers may not know their vehicle's speed, increasing crash risk. Tesla will provide a free software update.

    Product
    TESLA — 2020 TESLA MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V264000·2023-06-04

    2022 Tesla Model X: Missing Seat Reinforcement Bracket Safety Defect

    Tesla is recalling one 2022 Model X vehicle due to a missing body structure reinforcement bracket at the second-row seat. This failure to comply with federal seat restraint standards increases the risk of occupant injury in a crash.

    Product
    TESLA — 2022 TESLA MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V306000·2023-06-04

    Tiffin Bus and Phaeton motorhomes recalled for fuel rail leakage and fire risk

    Tiffin Motorhomes is recalling 2017-2021 Bus and Phaeton vehicles due to fuel rail assembly defects that may leak, posing a fire risk. Owners should contact Tiffin customer service at 1-256-356-8661 for a free inspection.

    Product
    TIFFIN — 2021 TIFFIN BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V252000·2023-06-04

    2022–2023 Land Rover Range Rover Seat Frame Defect Recall

    Jaguar Land Rover North America is recalling certain 2022–2023 Land Rover Range Rover vehicles because the second-row left seat frame may have been insufficiently welded and may not adequately secure occupants during crashes or sudden braking.

    Product
    LAND ROVER — 2022 LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V146000·2023-06-03

    2023 Triumph Bonneville T120 motorcycles recalled for brake disc detachment risk

    Triumph is recalling certain 2023 Bonneville T120 motorcycles because the left-hand side brake disc may detach, reducing brake performance and increasing crash risk. Dealers will install replacement parts free of charge.

    Product
    TRIUMPH — 2023 TRIUMPH BONNEVILLE T120
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V221000·2023-06-03

    2021 Alfa Romeo Stelvio Side Curtain Air Bag May Fail to Deploy

    2021 Alfa Romeo Stelvio vehicles may have improperly crimped clamps in the side curtain air bag assembly, which can fail to deploy in a crash, increasing injury risk. Chrysler will replace the assemblies at no cost.

    Product
    ALFA ROMEO — 2021 ALFA ROMEO STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V223000·2023-06-03

    2020-2021 Lincoln Aviator vehicles recalled for backup camera display failure

    Ford is recalling 2020-2021 Lincoln Aviator vehicles because the backup camera display may not show video feed, affecting rear visibility. Free software updates are available from Ford dealers.

    Product
    LINCOLN — 2020 LINCOLN AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23213·2023-06-01

    PowerXL Self-Cleaning Juicers recalled for laceration and ingestion hazards

    Empower Brands is recalling about 469,000 PowerXL Self-Cleaning Juicers because they can rupture during use, causing cuts, or leave particle shavings in juice. The company is aware of 261 incident reports including 47 injuries.

    Product
    PowerXL Self-Cleaning Juicers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23212·2023-06-01

    EGO Power+ Cordless Hedge Trimmers recalled for unexpected activation and laceration risk

    Chervon North America is recalling about 85,000 EGO Power+ Model HT2410 Cordless Brushless Hedge Trimmers due to a faulty rear trigger switch. The company has received 34 reports of unexpected activation, including 8 that caused lacerations requiring stitches.

    Product
    EGO Power+ Model HT2410 Cordless Brushless Hedge Trimmers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V016000·2023-06-01

    2022 Peterbilt 579 chassis step bolts may loosen and cause injury

    Bolts securing the chassis fairing step assembly on certain 2022 Peterbilt 579 vehicles may loosen and fracture. This can cause the step to move unexpectedly while entering or exiting the cab, increasing the risk of injury.

    Product
    PETERBILT — 2022 PETERBILT 579
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·23211·2023-06-01

    Jetson Nova and Star 3-Wheel Kick Scooters Recalled for Fall Hazard

    Jetson Electric Bikes is recalling about 15,300 Nova and Star 3-Wheel Kick Scooters because the rear wheel can loosen or fall off, posing a fall hazard to children. The company has received 12 reports of wheel loosening or falling, including one injury.

    Product
    Jetson Nova and Star 3-Wheel Kick Scooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1594-2023·2023-05-31

    COVID-19 At-Home Test Kits Recalled for Bacterial Buffer Contamination

    SD Biosensor is recalling 2,712,767 Pilot COVID-19 At-Home Test kits nationwide due to bacterial contamination in the liquid buffer component. Users may notice an odor from affected kits.

    Product
    Pilot COVID-19 At-Home Test, Reference Number 9901-NCOV-10G, Catalog Number 99COV200L-EN02, UPC Code: 887473000207 (EAN-13: 08800111707728)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0712-2023·2023-05-31

    dilTIAZem Injectable Bags Recalled Nationwide for Sterility Concerns

    Central Admixture Pharmacy Services is recalling 1,230 bags of dilTIAZem injectable due to lack of sterility assurance following FDA inspection. Affected lots were distributed nationwide.

    Product
    dilTIAZem added to dextrose 5%, 125 mg/125 mL* (1 mg/mL), 125 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 72185-6054-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0748-2023·2023-05-31

    Vasopressin Injectable Recalled Due to Sterility Assurance Failure

    Central Admixture Pharmacy Services is recalling vasopressin 40 units injectable because FDA inspection raised concerns about sterility assurance.

    Product
    vasopressin 40 units added to 0.9% sodium chloride 100 mL*, 0.4 units/mL*, 100 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-9001-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0653-2023·2023-05-31

    FDA Recalls Cardioplegia Solution Over Sterility Assurance Concerns

    Central Admixture Pharmacy Services is recalling Cardioplegia Solution, Reperfusate 4:1 due to lack of sterility assurance identified during an FDA inspection. The recall affects 338 bags distributed nationwide.

    Product
    Cardioplegia Solution, Reperfusate 4:1 low potassium, 15 mEq K, packaged in 477.5 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0008-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0726-2023·2023-05-31

    FDA Recalls Heparin-Sodium Chloride Injection Nationwide for Sterility Assurance Failure

    Central Admixture Pharmacy Services is recalling 3,055 bags of heparin injection nationwide due to sterility assurance concerns identified during FDA inspection. Healthcare providers and patients should discontinue use of affected lots.

    Product
    heparin added to 0.9% sodium chloride, 7,500 units/1,000 mL* (7.5 units/mL), 1000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7009-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0751-2023·2023-05-31

    Injection Solution Recalled Due to Sterility Assurance Concerns

    Nationwide recall of Sodium Phosphates Injection due to lack of sterility assurance after FDA inspection. Patients receiving this medication should consult their healthcare provider.

    Product
    Sodium Phosphates Injection 4 mEq/3 mMol/mL, 500 ml bag, Rx only, Central Admixture Pharmacy Services, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-8077-1, code 7128580771.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0669-2023·2023-05-31

    Cardioplegia Solution Recalled for Lack of Sterility Assurance

    Central Admixture Pharmacy Services recalls Cardioplegia Solution (182 bags, nationwide distribution) due to lack of sterility assurance identified during FDA inspection.

    Product
    Cardioplegia Solution, Modified St Thomas Solution, low potassium, HIGH SODIUM BICARBONATE, 62 mEq K, packaged in 1000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0203-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0723-2023·2023-05-31

    Drug Recall: Vancomycin Injectable Lacks Sterility Assurance

    Central Admixture Pharmacy Services recalls 7,632 bags of vancomycin injectable (NDC 71285-6078-1) nationwide due to FDA-identified sterility assurance deficiency.

    Product
    vancomycin added to 0.9% sodium chloride, 2 g/500 mL* (4 mg/mL), 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6078-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0655-2023·2023-05-31

    Cardioplegia Solution Recalled for Lack of Sterility Assurance

    Central Admixture Pharmacy Services is recalling a cardioplegia solution used in cardiac surgery due to lack of assured sterility following an FDA inspection. The product poses a potential infection risk to surgical patients.

    Product
    Cardioplegia Solution, Warm Induction 4:1 HIGH POTASSIUM/low tromethamine, 40 mEq K, packaged in 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0011-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0721-2023·2023-05-31

    Vancomycin and Dextrose Injection Sterility Recall by Central Admixture

    Central Admixture Pharmacy Services recalls 10,282 bags of vancomycin in dextrose 5% nationwide after FDA inspection raised sterility assurance concerns for this injectable pharmaceutical product.

    Product
    vancomycin added to dextrose 5%, 1.5 g/250 mL* (6 mg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6075-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0680-2023·2023-05-31

    Cardioplegia Solution Recalled Nationwide Due to Unverified Sterility

    Central Admixture Pharmacy Services is recalling 79 bags of Cardioplegia Solution nationwide because an FDA inspection found that the sterility of the product could not be assured.

    Product
    Cardioplegia Solution, LEESBURG CARDIOPLEGIA, packaged in 1030.2 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., Lehigh Valley, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-0218-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0771-2023·2023-05-31

    Compounded Tirzepatide Injections Recalled Nationwide Due to Sub-Potency

    Revive Rx is recalling 45 vials of compounded tirzepatide 10 mg/0.5 mL injections nationwide due to sub-potency. Patients should contact their healthcare provider about their medication.

    Product
    Tirzepatide 10 mg/0.5 mL Sterile Solution-2 mL Vial, Rx Only, For Sub-Q Use Only, Compounded Drug Product By: Revive Rx, 3831 Golf Dr A, Houston, TX 77018, NDC: 99000-9278-64.
    Category
    Drug
    Distribution
    Distributed nationwide