The Recall Desk

State

Utah product recalls

72,986 recalls have nationwide distribution and so reach Utah. 4,902 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total
4,902
Critical
524
Severe
1,091
Most recent
2026-09-16

Of the 4,902 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 1,091 (22%) are Severe.

These figures cover only the 4,902 recalls whose distribution notice names Utah specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6576–6600 of 77888

  • HighFDA (Food)·F-0828-2025·2025-06-11

    Gluten-Free Cinnamon Raisin Bagels Recalled for Undeclared Egg Allergen

    NEW GRAINS GLUTEN FREE BAKERY is recalling Cinnamon Raisin Bagels (16 oz, 4-count packages) due to poor label printing that fails to clearly declare the presence of egg allergen.

    Product
    Cinnamon Raisin Bagels: Gluten-free cinnamon raisin bagels, clear plastic bag, 16 oz, 4 bagels/package Ingredients: White rice flour, Water, Egg whites, Raisins, Honey, Tapioca flour, Golden flax seed, Palm fruit oil, Potato flour, Yeast, Sugar, Cinnamon, Psyllium husk powder,
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1886-2025·2025-06-11

    Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack Recalled

    Mozarc Medical is recalling Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Packs due to a potential breach of sterile barrier packaging that could compromise the catheter's sterility.

    Product
    Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1896-2025·2025-06-11

    Signature Laparoscopic Sharp Tooth Grasper Insulation Defect Recall

    Silex Medical recalls the Signature Laparoscopic Sharp Tooth Grasper due to incomplete insulation on the shaft near the rotator wheel, which creates an electrical hazard during use.

    Product
    Signature Laparoscopic Instruments, Sharp Tooth Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5863020.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1894-2025·2025-06-11

    Signature Laparoscopic Allis Clamp Grasper with Rotating Shaft Recalled

    Silex Medical is recalling the Signature Laparoscopic Instruments Allis Clamp Grasper due to incomplete insulation on the shaft, leaving an exposed area that could pose an electrical hazard during surgical procedures.

    Product
    Signature Laparoscopic Instruments, Allis Clamp Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5862030.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0832-2025·2025-06-11

    Frosted Sugar Cookies Recalled for Undeclared Allergens

    New Grains Gluten Free Bakery is recalling Frosted Sugar Cookies because the label does not clearly declare allergens: Egg, Milk, and Soy. The product was distributed in Utah.

    Product
    Frosted Sugar Cookie: Gluten-free frosted sugar cookies, clear plastic bag, 4 oz, 6 cookies/package Ingredients: White rice flour, Powdered sugar, Butter, Sugar, Palm shortening, Sprinkles, Rice milk, Egg whites, Potato flour, Imitation vanilla, Baking powder, Xanthan gum, Gela
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0825-2025·2025-06-11

    Gluten-Free Sourdough Bread Recalled for Undeclared Egg Allergen

    NEW GRAINS GLUTEN FREE BAKERY is recalling Artisan Sourdough Bread (gluten-free, 32 oz) distributed in Utah because the label does not clearly declare the presence of egg allergen due to poor print quality.

    Product
    Artisan Sourdough Bread: Gluten-free sourdough bread, vacuum-sealed clear plastic, 32 oz, 1 loaf/package Ingredients: White rice flour, Water, Eggs, Tapioca flour, Sugar, Potato flour, Palm fruit oil, Yeast, Psyllium husk powder, Vinegar, Sea salt, Xanthan gum, Powdered sugar.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1900-2025·2025-06-11

    Signature Laparoscopic Atraumatic Grasper Insulation Defect Recall

    Silex Medical is recalling Signature Laparoscopic Instruments (Model 5881033) because insulation on the shaft does not fully extend to the proximal end, leaving an exposed area near the rotator wheel.

    Product
    Signature Laparoscopic Instruments, 20mm Atraumatic Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5881033.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0838-2025·2025-06-11

    Pecan Caramel Bars Recalled for Undeclared Allergen Labels

    New Grains Gluten Free Bakery is recalling Pecan Caramel Bars sold in Utah because printing quality issues made allergen declarations for egg, milk, and pecans unreadable or missing on the package.

    Product
    Pecan Caramel Bars Individually wrapped in plastic. Ingredients: White rice flour, Sugar, Honey, Pecan pieces, Butter, Eggs, Rice milk, Potato flour, Vanilla, Baking powder, Xanthan gum, Unflavored gelatin, Sea salt Contains: Egg, Milk, Tree nuts
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1910-2025·2025-06-11

    ChannelCheck Convenience Pack Pre-filled Water Syringes Recalled

    Healthmark Industries is recalling ChannelCheck Convenience Pack Pre-filled Water Syringes (Models UCC-222CP and UCC-222-ESP) because contamination was found in duodenoscope samples linked to the syringes, which were improperly used outside their intended purpose.

    Product
    ChannelCheck Convenience Pack, Model Numbers UCC-222CP and UCC-222-ESP (Sample)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1888-2025·2025-06-11

    Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack recalled

    Mozarc Medical is recalling Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack units due to a potential breach of sterile barrier packaging. The affected catheter models were distributed nationwide in the US and in Canada and Mexico.

    Product
    Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V365000·2025-06-11

    Mercedes-Benz Recalls 2023 GLC 300 Models for Missing Headlight Caps

    Mercedes-Benz is recalling 2023 GLC 300 and GLC 300 4MATIC vehicles because missing caps allow improper headlight adjustment, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 300, GLC 300 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1895-2025·2025-06-11

    Signature Laparoscopic Debakey Grasper Instruments Recalled for Insulation Defect

    Silex Medical is recalling 8 units of Signature Laparoscopic Debakey Grasper instruments (Model 5862100) due to incomplete insulation on the shaft near the rotator wheel, which could expose the user or patient to electrical contact.

    Product
    Signature Laparoscopic Instruments, Debakey Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5862100.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1887-2025·2025-06-11

    Palindrome Precision SI Chronic Hemodialysis Catheter Sterile Barrier Recall

    Mozarc Medical US LLC is recalling Palindrome Precision SI Chronic Hemodialysis Catheters (Sport Pack) due to a potential breach of sterile barrier packaging. Approximately 95,938 units distributed nationwide and in Canada and Mexico are affected.

    Product
    Palindrome Precision SI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0455-2025·2025-06-11

    Fluoxetine Tablets USP 20 mg Recalled for N-Nitroso Contamination

    Torrent Pharma Inc. is recalling Fluoxetine Tablets USP 20 mg due to the presence of N-Nitroso Fluoxetine exceeding the interim acceptable intake limit. The affected lot is distributed nationwide.

    Product
    FLUOXETINE — FLUOXETINE (FLUOXETINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1903-2025·2025-06-11

    Luminex VERIGENE Gram Negative Blood Culture Test Recalled

    Luminex is recalling VERIGENE Gram Negative Blood Culture test cartridges due to a consumable issue that may produce incorrect results on a small portion of one lot.

    Product
    VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test, REF 20-006-021; for use with the sample-to-results VERIGENE System; invitro diagnostic test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1889-2025·2025-06-11

    MAHURKAR Chronic Hemodialysis Catheter recalled for sterile barrier defect

    Mozarc Medical is recalling MAHURKAR Chronic Hemodialysis Catheter Sport Pack units due to a potential breach in sterile barrier packaging that could compromise the product's sterility.

    Product
    MAHURKAR Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1885-2025·2025-06-11

    Palindrome Precision Chronic Hemodialysis Catheter Sport Pack Recalled

    Mozarc Medical US LLC is recalling Palindrome Precision Chronic Hemodialysis Catheter Sport Pack units due to a potential breach of sterile barrier packaging. Affected units were distributed worldwide including the US, Canada, and Mexico.

    Product
    Palindrome Precision Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0837-2025·2025-06-11

    Dye-Free Frosted Sugar Cookies Recalled for Undeclared Allergens

    New Grains Gluten Free Bakery is recalling Dye-Free Frosted Sugar Cookies due to printing quality issues that failed to clearly declare allergens (egg, milk, soy) on the label. The product was distributed in Utah.

    Product
    Dye-Free Frosted Sugar Cookie: Gluten-free dye-free frosted sugar cookies, clear plastic bag, 4 oz, 6 cookies/package Ingredients: White rice flour, Powdered sugar, Butter, Sugar, Palm shortening, Sprinkles, Rice milk, Egg whites, Potato flour, Imitation vanilla, Baking powder,
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1898-2025·2025-06-11

    Signature Laparoscopic Alligator Grasper Instrument Recall Safety Issue

    Silex Medical is recalling the Signature Laparoscopic Alligator Grasper with Rotating Shaft (Model 5863050) because insulation on the tube does not fully extend to the proximal end of the shaft, leaving an exposed uninsulated area near the rotator wheel.

    Product
    Signature Laparoscopic Instruments, Alligator Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5863050.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1893-2025·2025-06-11

    Signature Laparoscopic Dolphin Nose Grasper Instrument Insulation Defect

    Silex Medical is recalling 2 units of a Signature Laparoscopic Instruments Dolphin Nose Grasper with Rotating Shaft due to incomplete insulation on the shaft, leaving an exposed area near the rotator wheel.

    Product
    Signature Laparoscopic Instruments, Dolphin Nose Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5860020.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1899-2025·2025-06-11

    Signature Laparoscopic Atraumatic Grasper Instrument Insulation Defect Recall

    Silex Medical is recalling Signature Laparoscopic Atraumatic Grasper instruments (Model 5864000) due to incomplete insulation on the shaft that leaves an exposed area near the rotator wheel, posing an electrical safety risk during surgical use.

    Product
    Signature Laparoscopic Instruments, Atraumatic Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5864000.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1906-2025·2025-06-11

    Dexcom G7 iOS App version 2.7.0 stops updating glucose readings

    Dexcom G7 iOS App version 2.7.0 can enter a state where glucose readings freeze and alerts do not trigger, risking missed detection of dangerously high or low blood sugar. Other connected devices like Apple Watch and insulin pumps continue to receive glucose data directly from the transmitter.

    Product
    Dexcom G7 iOS Application, Ref: SW12300 used in conjunction with the Dexcom G7 Continuous Glucose Monitoring (CGM) system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0829-2025·2025-06-11

    Plain Gluten-Free Bagels Recalled for Undeclared Egg Allergen

    NEW GRAINS GLUTEN FREE BAKERY is recalling plain gluten-free bagels due to printing quality issues that rendered the egg allergen declaration unclear or unreadable on the label.

    Product
    Plain Bagels: Gluten-free plain bagels, clear plastic bag, 16 oz, 4 bagels/package Ingredients: White rice flour, Water, Egg whites, Tapioca flour, Sugar, Palm fruit oil, Potato flour, Yeast, Rice bran, Psyllium husk powder, Sea salt, Xanthan gum, Enzyme. Contains: Egg.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0827-2025·2025-06-11

    Gluten-Free Blueberry Bagels Recalled for Undeclared Egg Allergen

    New Grains Gluten Free Bakery is recalling gluten-free blueberry bagels because the label does not clearly declare the egg allergen due to printing quality issues.

    Product
    Blueberry Bagels: : Gluten-free blueberry bagels, clear plastic bag, 16 oz, 4 bagels/package Ingredients: White rice flour, Water, Egg whites, Tapioca flour, Sugar, Palm fruit oil, Potato flour, Yeast, Rice bran, Psyllium husk powder, Sea salt, Xanthan gum, Enzyme. Contains: Eg
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0830-2025·2025-06-11

    Gluten-Free Multigrain Bagels Recalled for Undeclared Egg Allergen

    NEW GRAINS GLUTEN FREE BAKERY is recalling gluten-free multigrain bagels due to printing defects that render the egg allergen declaration illegible on the package label. The product contains egg and poses a risk to consumers with egg allergies.

    Product
    Multigrain Bagels: Gluten-free multigrain bagels, clear plastic bag, 16 oz, 4 bagels/package Ingredients: White rice flour, Water, Egg whites, Tapioca flour, Honey, Golden flax seed, Palm fruit oil, Potato flour, Yeast, Sugar, Psyllium husk powder, Rice bran, Sea salt, Xanthan
    Category
    Food
    Distribution
    1 state