The Recall Desk

State

Utah product recalls

73,833 recalls have nationwide distribution and so reach Utah. 4,916 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total
4,916
Critical
524
Severe
1,351
Most recent
2026-11-04

Of the 4,916 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 1,351 (27%) are Severe.

Which agencies issued them

These figures cover only the 4,916 recalls whose distribution notice names Utah specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53501–53525 of 78749

  • SevereFDA (Food)·F-0737-2016·2016-03-16

    Kroger Recalls King Soopers Gourmet Bread Pudding for Undeclared Walnuts

    The Kroger Co is recalling King Soopers City Market Gourmet Bread Pudding due to undeclared walnuts. The product was distributed in Colorado and Utah.

    Product
    King Soopers City Market GOURMET BREAD PUDDING; Various Sizes, INGREDIENTS: HALF & HALF***APPLES, LIQUID EGG***SPICES, SALT***RAISINS, CINNAMON. CONTAINS EGG, MILK, SOY, WHEAT; UPC 2 47460 0XXXX
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0744-2016·2016-03-16

    Hartley Medical Center Pharmacy Recalls Morphine and Bupivacaine Syringes

    Hartley Medical Center Pharmacy is recalling Morphine Sulfate and Bupivacaine HCL syringes due to a lack of assurance of sterility.

    Product
    Morphine Sulfate 20 mg/ml/Bupivacaine HCL 11.3 mg/ml, vol. 40 ml syringe, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0752-2016·2016-03-16

    Hartley Medical Center Pharmacy Recalls Hydromorphone Syringes Due to Sterility Concerns

    Hartley Medical Center Pharmacy is recalling Hydromorphone HCL 10 mg/ml syringes due to a lack of assurance of sterility. The product was distributed nationwide.

    Product
    Hydromorphone HCL 10 mg/ml, vol. 40 ml syringe, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1062-2016·2016-03-16

    Arrow Percutaneous Insertion Tray Recalled for Potential Sheath Separation

    Arrow International is recalling specific Percutaneous Insertion Trays because the sheath body may separate from the hub, posing a risk of bleeding.

    Product
    Percutaneous Insertion Tray; Product Code: IAK-06845 The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0765-2016·2016-03-16

    Hartley Medical Center Pharmacy Recalls Sufentanil Citrate Syringes Due to Sterility Concerns

    Hartley Medical Center Pharmacy is recalling Sufentanil Citrate/Clonidine/Bupivacaine syringes because the agency could not ensure the product was sterile.

    Product
    Sufentanil Cit 50 mcg/ml/Clonidine HCL 1 mcg/ml/Bupivacaine HCL 5 mg/ml, vol. 20 ml syringe, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0741-2016·2016-03-16

    Hartley Medical Center Pharmacy Recalls Morphine Sulfate Combination Vials

    Hartley Medical Center Pharmacy is recalling Morphine Sulfate, Sufentanil Citrate, and Bupivacaine HCL vials due to a lack of assurance of sterility.

    Product
    Morphine Sulfate 9 mg/ml/Sufentanil Cit 180 mcg/ml/Bupivacaine HCL 33 mg/ml, vol. 20 ml vial, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1076-2016·2016-03-16

    BD Intelliport Medication Management System Sensor Recalled for Sterility Concerns

    Becton Dickinson is recalling 250 units of the BD Intelliport Medication Management System Sensor because the sterility of the product cannot be assured, posing an increased risk of infection.

    Product
    BD Intelliport Medication Management System Sensor The system is indicated for use by healthcare professionals in a hospital or medical center setting with patients who are receiving manually administered bolus intravenous injections as part of their care to facilitate…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1068-2016·2016-03-16

    Bard Denali Filter Delivery System Recalled for Cracking Stop Cocks

    Bard Peripheral Vascular is recalling Denali Filter Delivery Systems because stop cocks may crack.

    Product
    Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J; Indicated for use in the prevention of recurrent pulmonary embolism via placement in the vena cava.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1065-2016·2016-03-16

    Philips Respironics Recalls Trilogy and Garbin Ventilators Due to Software Issue

    Philips Respironics is recalling approximately 104,508 Trilogy and Garbin ventilators due to a software issue. The recall covers units distributed nationwide and internationally.

    Product
    Trilogy 100, Trilogy 200, Trilogy O2, Trilogy 202, Trilogy EC, Garbin, Garbin Plus Trilogy 100, Trilogy 200, Garbin, Garbin plus provides continuous or intermittent ventilatory support for the care of individuals who require mechanical ventilation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0744-2016·2016-03-16

    Urban Oven Cookies Recalled for Undeclared Milk Allergen

    Urban Oven, LLC is recalling four varieties of cookies because the label fails to declare milk, an ingredient present in the butter used.

    Product
    Urban Oven Artisan-Baked Short Bread Cookies Pecan All Natural NET. WT. 5 oz. UPC Code: 7 18122 06364 2 SKU #: C3000
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1084-2016·2016-03-16

    Sedecal Mobile X-ray Systems Recalled for Uncommanded Movements

    Sedecal S.A. is recalling 349 mobile X-ray systems because static electricity and other issues can cause uncommanded movements.

    Product
    Mobile wDR motorized portable diagnostic X-ray systems. Intended for use by a qualified/trained doctor or technologist on both adult and pediatric patients for taking diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, and other body…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16122·2016-03-16

    SRAM Recalls Zipp Bicycle Wheel Hubs Due to Crash and Injury Hazards

    SRAM is recalling Zipp 88 aluminum front hubs because the flanges can fail, posing a crash and injury hazard. Consumers should stop using the hubs and contact SRAM for a free replacement.

    Product
    Zipp 88 aluminum front hubs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1064-2016·2016-03-16

    Arrow Recalls Percutaneous Sheath Introducer Sets Due to Packaging Damage

    Arrow International Inc. is recalling Super Arrow-Flex Percutaneous Sheath Introducer Sets because packaging damage may compromise sterility, posing a potential infection risk.

    Product
    Super Arrow-Flex Percutaneous Sheath Introducer Sets REF CL-07035 or CL-07635 or CL-07735 or CL-07835 Super Arrow-Flex Percutaneous Sheath Introducer Set with Integral Hemostasis Valve/Side Port and Radiopaque Tip Marker Band Contents: 1: . . . . . . . . . Sheath*: ***…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V154000·2016-03-16

    Terex Recalls Aerial Devices Due to Suspension Air Bag Defect

    Terex is recalling 2015-2016 aerial devices and digger derrick lifts because the suspension circuit can inflate air bags, lifting outriggers and increasing injury risk.

    Product
    TEREX — TEREX TM125, HRX, C5000, C6000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0745-2016·2016-03-16

    Urban Oven Cookies Recalled for Undeclared Milk Allergen

    Urban Oven, LLC is recalling specific cookie varieties because the label fails to declare milk, an ingredient present in the butter used.

    Product
    Urban Oven Artisan-Baked Short Bread Cookies Lemon Pistachio All Natural NET WT. 5 oz UPC Code: 7 18122 06374 1 SKU #: C4000
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0724-2016·2016-03-16

    Maesri Shrimp Powder Recalled for Undeclared Yellow #6 Dye

    Eastland Food Corporation is recalling Maesri Brand Shrimp Powder because it contains FD&C Yellow #6, which is not listed on the label.

    Product
    Maesri Brand Shrimp Powder, 6.oz
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1069-2016·2016-03-16

    Bard Denali Filter Delivery Systems Recalled for Cracking Stop Cocks

    Bard Peripheral Vascular is recalling Denali Filter Delivery Systems because stop cocks may crack.

    Product
    Denali Filter-Femoral Delivery System Product Code: DL900F/DL950F; Indicated for use in the prevention of recurrent pulmonary embolism via placement in the vena cava.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16120·2016-03-16

    GE Lighting Recalls High-Intensity LED Lamps Due to Impact Hazard

    GE Lighting is recalling high-intensity LED lamps because they can separate from their base and fall, posing an impact hazard. No injuries have been reported.

    Product
    High-intensity LED lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1082-2016·2016-03-16

    Biomet Recalls Crosslock DVR ePAK Surgical Sets Due to Oxidation Risk

    Biomet is recalling 21,268 Crosslock DVR ePAK surgical sets because components may oxidize during storage. This could cause an inflammatory reaction if material enters the surgical wound.

    Product
    Crosslock DVR ePAK -Sterile, Ref 81180050, are complete surgical sets including plates, screws, and instruments for orthopedic fixation The Cross lock DVR ePAK Volar Rim Plates system is intended for fixation of fractures, mal unions, and osteotomies involving the distal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0743-2016·2016-03-16

    Urban Oven Cookies Recalled for Undeclared Milk Allergen

    Urban Oven, LLC is recalling specific cookie varieties because the label fails to declare milk, an ingredient present in the butter used.

    Product
    Urban Oven Artisan-Baked Short Bread Cookies Cocoa All Natural NET Wt. 5 oz. UPC Code: 7 18122 06354 3 SKU #: C2000
    Category
    Food
    Distribution
    7 states