The Recall Desk

State

Utah product recalls

72,907 recalls have nationwide distribution and so reach Utah. 4,901 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total
4,901
Critical
524
Severe
1,091
Most recent
2026-09-09

Of the 4,901 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 4,901 recalls whose distribution notice names Utah specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

976–1000 of 77808

  • SevereCPSC·26601·2026-07-02

    Metal Wire Bristle Grill Brushes Recalled Over Detachable Bristle Ingestion Hazard

    Conair is recalling about 1.7 million Cuisinart metal wire bristle grill brushes because small wire bristles can detach and be swallowed, posing a risk of serious internal injury. Three consumers have already swallowed bristles and required medical treatment.

    Product
    Metal Wire Bristle Grill Brushes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V426000·2026-07-02

    Jayco Recalls 2026 Seismic Fifth Wheel Toy Haulers Due to Fire Risk

    Jayco is recalling 2026 Seismic fifth wheel toy haulers because the inverter may lack a grounding connection, increasing the risk of fire and electrical shock.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL SEISMIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V431000·2026-07-02

    Kia Recalls EV6 and EV9 Models Due to Battery Fire Risk

    Kia is recalling 2022-2024 EV6 and 2024 EV9 vehicles because high voltage battery cells may contain misaligned electrodes, creating a fire hazard.

    Product
    KIA — KIA EV9, EV6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26603·2026-07-02

    Roman Candles 8 Shot Fireworks Recalled for Explosion and Burn Hazards

    Winco Fireworks International is recalling Roman Candles 8 Shot 3-Pack firework devices because the fireworks can malfunction and shots can blow out the side of the tube, posing a risk of serious injury from explosion and burn hazards. No injuries have been reported.

    Product
    Roman Candles 8 Shot 3-Pack Firework Devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26E041000·2026-07-02

    Warn Industries Recalls Wireless Remote Kits Due to Winch Movement Risk

    Warn Industries is recalling Wireless Remote Kits (part numbers 90287 and 90289) because the remote control may be incompatible with legacy winches, causing unexpected movement and increasing injury risk.

    Product
    EQUIPMENT:MECHANICAL:WINCH recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26594·2026-07-02

    POPOOO Jungle Safari LED Finger Lights Recalled for Battery Ingestion Risk

    CPSC has recalled POPOOO Jungle Safari LED Finger Lights sold on Amazon because the toys contain easily accessible button cell batteries that can cause serious injury or death if swallowed. No injuries have been reported.

    Product
    POPOOO Jungle Safari LED Finger Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26595·2026-07-02

    Rowenta Cordless Vacuum Cleaners Recalled for Fire and Burn Hazard

    Rowenta is recalling cordless vacuum cleaners with lithium-ion batteries that can overheat and ignite, posing a risk of fire and burn injury. About 3,660 units are affected; no injuries have been reported.

    Product
    Rowenta Cordless Vacuum Cleaners with lithium-ion battery
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26592·2026-07-02

    Topyond Pool Drain Ports with Covers Recalled for Entrapment Risk

    Topyond pool drain ports with covers violate federal entrapment protection standards and pose serious injury or death risks from entrapment and drowning. Consumers should stop using pools with these drain ports immediately.

    Product
    Topyond Pool Drain Port with Cover
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26598·2026-07-02

    Gigglescape Under the Sea Popping Toy Recalled for Choking Hazard

    Target has recalled approximately 49,000 Gigglescape Under the Sea Popping Toys because the clear plastic dome can detach, exposing small plastic balls that pose a choking hazard. One child began to choke after the dome detached.

    Product
    Gigglescape™ Under the Sea Popping Toy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26602·2026-07-02

    Unity 7 Shot 200 Gram Aerial Cake Fireworks Recalled for Explosion and Burn Hazard

    Winco Fireworks International recalls Unity 7 Shot 200 Gram Aerial Cake firework devices that can tip over, creating risk of serious injury from explosion and burns. About 87,120 units sold at Pyro City and independent fireworks stores nationwide from January through May 2026 are affected.

    Product
    Unity 7 Shot 200 Gram Aerial Cake Firework Devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26596·2026-07-02

    AMASKY Nursing Pillows Recalled for Risk of Suffocation

    AMASKY Nursing Pillows, sold on Amazon from January to March 2026, violate safety standards and can obstruct infant breathing, posing a serious risk of suffocation. No injuries have been reported.

    Product
    AMASKY Nursing Pillows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2525-2026·2026-07-01

    VOCSN+Pro Respiratory System Backup Battery Alarm Failure Recall

    Ventec Life Systems is recalling VOCSN+Pro respiratory systems due to a damaged backup battery that may prevent the backup alarm from activating during power loss, delaying caregiver awareness of a hazardous condition.

    Product
    VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1106-2026·2026-07-01

    Spring & Mulberry Blood Orange Date-Sweetened Chocolate recalled for Salmonella

    Spring & Mulberry Inc. is recalling Blood Orange Date-Sweetened Chocolate bars due to potential Salmonella contamination. Affected products were distributed nationwide.

    Product
    Spring & Mulberry Blood Orange Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in an orange box, UPC 850055470200, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold in
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1100-2026·2026-07-01

    Spring & Mulberry Mango Chili Date-Sweetened Chocolate bars recalled

    Spring & Mulberry Inc. is recalling Spring & Mulberry Mango Chili Date-Sweetened Chocolate bars nationwide due to potential Salmonella contamination. Consumers should not consume the product and should dispose of it or return it.

    Product
    Spring & Mulberry Mango Chili Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in an orange box, UPC 850055470033, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold indi
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2453-2026·2026-07-01

    Medline Convenience Kits with Lidocaine and Bupivacaine Injections Recalled

    Medline Industries is recalling 22 models of Convenience Kits that contain Lidocaine Hydrochloride Injection and Bupivacaine Hydrochloride in Dextrose Injection due to quality issues found during an FDA inspection of the supplier.

    Product
    Medline Convenience Kits: 1) OPEN HEART CDS, Model Number: CDS840144Q; 2) OPEN HEART, Model Number: CDS840150W; 3) OPEN HEART ADULT, Model Number: CDS840396AA; 4) CABG A CDS, Model Number: CDS982269N; 5) OPEN HEART ANESTHESIA PACK, Model Number: CDS983849G; 6) OPEN HE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2558-2026·2026-07-01

    Surgify Halo 4.0mm Extendable Surgical Burr Recall for Breakage Risk

    Surgify Medical is recalling Surgify Halo 4.0 mm Extendable surgical burrs due to potential breakage during bi-portal endoscopic spinal surgery. The breakage could create a safety hazard during the procedure.

    Product
    Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.H1; drills, burrs, trephines & accessories (simple, powered)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2602-2026·2026-07-01

    Abiomed Impella CP Set with SmartAssist 10th Generation Introducer Kit Recall

    Abiomed is recalling Impella CP Set with SmartAssist (10th Generation) containing 14Fr Low Profile Introducer Kits due to potential thrombus (blood clot) formation during prolonged use of the introducer.

    Product
    Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low Profile Introducer Kits 13 and 25 cm Japan. Product Code: 1000542.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0625-2026·2026-07-01

    ChloraPrep One-Step Antiseptic Solution Recall Due to Sterility Concerns

    CareFusion is recalling 178,000 ChloraPrep One-Step antiseptic applicators (Lot #4073005) nationwide due to potential non-sterility from fungal contamination and seal breaches from paper lidding wrinkles.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1104-2026·2026-07-01

    Spring & Mulberry Sea Salt Date-Sweetened Chocolate recalled for Salmonella

    Spring & Mulberry Inc. is recalling Sea Salt Date-Sweetened Chocolate bars due to potential Salmonella contamination. Approximately 9,932 individual bars distributed nationwide are affected.

    Product
    Spring & Mulberry Sea Salt Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a grey box, UPC 850055470071, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individua
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2590-2026·2026-07-01

    Medical Device Convenience Kits with 10mL Polycarbonate Syringes Recalled

    Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside FDA-cleared specifications. The recall affects approximately 113,843 kits distributed nationwide.

    Product
    Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. CATARACT FULL BODY DYNJ85743 MAJOR VASCULAR PACK DYNJ81610C MINIMALLY INVASIVE PACK-LF DYNJ0843063L PEDIATRIC CATH ANGIO PACK DYNJ54755J PERIPHERAL ARTERIOGRAM RAD DY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2601-2026·2026-07-01

    Abiomed Impella CP Set with SmartAssist 10th Generation Introducer Kits Recalled

    Abiomed is recalling certain Impella CP Set with SmartAssist (10th Generation) units with affected 14Fr Low Profile Introducer Kits due to potential for thrombus (blood clot) formation during prolonged use.

    Product
    Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low Profile Introducer Kits. Product Codes: 1000413, 1000834.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1102-2026·2026-07-01

    Spring & Mulberry Pecan Date Chocolate Recalled for Salmonella Risk

    Spring & Mulberry Inc. is recalling approximately 79,156 individually packaged pecan date date-sweetened chocolate bars nationwide due to potential Salmonella contamination.

    Product
    Spring & Mulberry Pecan Date Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a yellow box, UPC 850055470040, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold indiv
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1099-2026·2026-07-01

    Spring & Mulberry Lavender Rose Chocolate Recalled for Salmonella

    Spring & Mulberry Inc. is recalling Spring & Mulberry Lavender Rose Date-Sweetened Chocolate bars due to potential Salmonella contamination. The recall affects multiple batch lots distributed nationwide.

    Product
    Spring & Mulberry Lavender Rose Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a light blue box, UPC 850055470019, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold
    Category
    Food
    Distribution
    Distributed nationwide