The Recall Desk

State

Utah product recalls

72,984 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 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6551–6575 of 77886

  • SevereCPSC·25337·2025-06-12

    Oliver & Smith 6-inch Mattresses Recalled for Fire Hazard Risk

    Agro Superior Group is recalling about 16,530 Oliver & Smith 6-inch mattresses sold online because they violate federal flammability standards and pose a risk of serious injury or death from fire. Consumers should stop using them immediately.

    Product
    Oliver & Smith 6-inch Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25335·2025-06-12

    Skywalker Pro Via Ferrata Sets recalled due to fall-hazard risk

    Mammut Sports Group is recalling Skywalker Pro Via Ferrata Sets because the carabiner can open without engaging the safety latch, creating a risk of serious injury or death from falls.

    Product
    Skywalker Pro Via Ferrata Sets, Skywalker Pro Turn Via Ferrata Sets and Skywalker Pro Via Ferrata Packages
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25339·2025-06-12

    Manual Retractable Pool Covers Recalled for Drowning and Entrapment Hazards

    Endless Pools is recalling about 11,500 Manual Retractable Security Pool Covers because improper installation can leave gaps larger than 4.5 inches, posing drowning and entrapment risks to children.

    Product
    Manual Retractable Security Pool Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V392000·2025-06-12

    Volvo electric and hybrid models can lose braking in one-pedal mode

    Volvo is recalling certain electric and plug-in hybrid models because the vehicle may lose brake function while coasting downhill in "B" mode or One Pedal Drive. Owners are told not to use those modes until repaired.

    Product
    VOLVO — VOLVO S60PHEV, XC40BEV, S90PHEV, V60PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25336·2025-06-12

    Bugaboo Giraffe Highchairs Recalled for Fall Hazard Risk

    Bugaboo North America is recalling about 18,280 Giraffe highchairs because the legs can detach from the frame if screws are not properly tightened during assembly, posing a risk of serious injury or death. The company has received 22 reports of leg detachment, including 13 reports of minor injuries.

    Product
    Giraffe highchairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25338·2025-06-12

    Anker PowerCore 10000 Power Banks Model A1263 Recalled for Fire and Burn Hazards

    Approximately 1,158,000 Anker PowerCore 10000 power banks (model A1263) are recalled because their lithium-ion batteries can overheat, creating fire and burn hazards. Anker has received 19 reports of fires and explosions, including property damage totaling over $60,700.

    Product
    Anker PowerCore 10000 power banks (model A1263 only)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V390000·2025-06-12

    Chevrolet Silverado medium duty brake pressure switches may short and overheat

    GM is recalling certain 2019-2024 Chevrolet Silverado Medium Duty trucks because the brake pressure sensor may leak fluid into the switch and short circuit. Owners are told to park outside.

    Product
    CHEVROLET — CHEVROLET SILVERADO 4500, SILVERADO 6500, 6500, duplicate SILVERADO 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25334·2025-06-12

    RYOBI 40V 24-Inch Cordless Hedge Trimmers Recalled for Laceration Hazard

    TI Outdoor Power Equipment is recalling about 113,000 RYOBI 40V 24-inch cordless hedge trimmers because the blade can unexpectedly activate from pressing only one control, causing lacerations. Consumers should stop using the trimmer and return it for a free replacement.

    Product
    RYOBI 40V 24-Inch Cordless Hedge Trimmers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1814-2025·2025-06-11

    Adult Manual Resuscitator with Medium Adult Mask recalled nationwide

    SunMed Holdings is recalling 11,358 Adult Manual Resuscitators because the filter may be incorrectly attached to the patient port instead of the exhalation port, risking interruption or delay in patient resuscitation that could cause serious harm or death.

    Product
    Adult Manual Resuscitator with Medium Adult Mask, Bag REservoir, Filter, Manometer and 7 ft Oxygen Tubing, REF CPRM1116F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0833-2025·2025-06-11

    Gluten-Free Coconut Macaroon Cookies Recalled for Undeclared Allergens

    NEW GRAINS GLUTEN FREE BAKERY is recalling approximately 50 units of Coconut Macaroon Cookies because label printing quality issues rendered allergen declarations for Egg, Milk, and Soy illegible or missing.

    Product
    Coconut Macaroon Cookie: Gluten-free coconut macaroon cookies, clear plastic bag, 4 oz, 6 cookies/package Ingredients: Coconut flakes, Sweetened condensed milk, Egg whites, Potato flour, Vanilla, Sea salt. Contains: Egg, Milk, Soy.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0456-2025·2025-06-11

    Fluoxetine Tablets 20 mg Recalled for N-Nitroso Impurity

    Torrent Pharma Inc. is recalling Fluoxetine Tablets, USP, 20 mg in a 28-count carton due to the presence of N-Nitroso Fluoxetine exceeding the interim acceptable intake limit.

    Product
    FLUOXETINE — FLUOXETINE (FLUOXETINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0831-2025·2025-06-11

    Gluten-Free Chocolate Chip Cookies Recalled for Undeclared Allergens

    New Grains Gluten Free Bakery is recalling gluten-free chocolate chip cookies because printing quality issues rendered allergen declarations unreadable. The products contain egg, milk, and soy but do not clearly declare these allergens on the label.

    Product
    Chocolate Chip Cookie: Gluten-free brownie chocolate chip cookies, clear plastic bag, 4 oz, 8 cookies/package Ingredients: White rice flour, Butter, Chocolate chips, Brown sugar, Eggs, Sugar, Tapioca flour, Potato flour, Rice bran, Vanilla, Xanthan gum. Contains: Egg, Milk, Soy
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0835-2025·2025-06-11

    Artisan Seasoned Croutons Recalled Due to Undeclared Allergens

    New Grains Gluten Free Bakery is recalling Artisan Seasoned Croutons because printing quality issues made allergen declarations for Egg and Milk illegible or missing on the packaging.

    Product
    Artisan Seasoned Croutons: Gluten-free artisan seasoned croutons, vacuum-sealed clear plastic, 8 oz, bulk Ingredients: White rice flour, Water, Egg, Golden flax seed, Rice bran, Tapioca flour, Honey, Palm fruit oil, Potato flour, Yeast, Xanthan gum, Psyllium husk powder, Sea sa
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0836-2025·2025-06-11

    Seasoned Bread Crumbs Recalled for Undeclared Egg and Milk Allergens

    New Grains Gluten Free Bakery is recalling seasoned bread crumbs because printing quality issues made egg and milk allergen declarations illegible on the label. Consumers with allergies to these ingredients may face serious health risks.

    Product
    Seasoned Bread Crumbs: Gluten-free seasoned bread crumbs, vacuum-sealed clear plastic, 8 oz, bulk Ingredients: White rice flour, Water, Egg, Golden flax seed, Rice bran, Tapioca flour, Honey, Palm fruit oil, Potato flour, Yeast, Xanthan gum, Psyllium husk powder, Sea salt, Butt
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0826-2025·2025-06-11

    Artisan Cinnamon Raisin Bread Recalled for Undeclared Egg Allergen

    New Grains Gluten Free Bakery is recalling Artisan Cinnamon Raisin Bread because the label does not clearly declare the presence of egg allergen due to printing quality issues. The product contains egg and poses a risk to people with egg allergies.

    Product
    Artisan Cinnamon Raisin Bread: Gluten-free cinnamon raisin bread, vacuum-sealed clear plastic, 32 oz, 1 loaf/package Ingredients: White rice flour, Water, Egg whites, Raisins, Honey, Tapioca flour, Golden flax seed, Palm fruit oil, Potato flour, Yeast, Sugar, Cinnamon, Psyllium
    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
  • 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-0824-2025·2025-06-11

    Gluten-Free Artisan White Bread Recall Due to Undeclared Egg Allergen

    New Grains Gluten Free Bakery is recalling approximately 41 units of Artisan White Bread due to undeclared egg allergen on the label. Poor print quality rendered the egg allergen declaration illegible or missing.

    Product
    Artisan White Bread: Gluten-free artisan white bread, vacuum-sealed clear plastic, 32 oz, 1 loaf/package Ingredients: White rice flour, Water, Egg whites, Tapioca flour, Sugar, Palm oil, Potato flour, Yeast, Rice bran, Psyllium husk powder, Sea salt, Xanthan gum. Contains: Egg.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1897-2025·2025-06-11

    Signature Laparoscopic Bullet Tip Grasper Instrument Insulation Defect Recall

    Silex Medical is recalling 6 units of the Signature Laparoscopic Bullet Tip Grasper with Rotating Shaft due to incomplete insulation on the shaft near the rotator wheel, which could expose users to electrical hazards.

    Product
    Signature Laparoscopic Instruments, Bullet Tip Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5863030.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0928-2025·2025-06-11

    GNC Women's 30+ Vitapak recalled due to undeclared fish allergen

    GNC Holdings LLC is recalling GNC Women's 30+ Vitapak due to undeclared fish allergen (parvalbumin). The product was distributed across multiple states.

    Product
    GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet contains four tablets and a capsule. Paper-board carton that measures 10.25 width x 3.56 height x 3.15 depth containing 30 sachets of 3 width x 2.75 height with tear notch. 15 Cartons per Case
    Category
    Food
    Distribution
    48 states
  • 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-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