The Recall Desk

State

Utah product recalls

73,738 recalls have nationwide distribution and so reach Utah. 4,914 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total
4,914
Critical
524
Severe
1,350
Most recent
2026-10-28

Of the 4,914 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 1,350 (27%) are Severe.

Which agencies issued them

These figures cover only the 4,914 recalls whose distribution notice names Utah specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31451–31475 of 78652

  • LowFDA (Drugs)·D-1049-2020·2020-04-01

    FDA Recalls Colostat Homeopathic Remedy Due to Incorrect Labeling

    Grato Holdings, Inc. is recalling 659 bottles of Colostat homeopathic remedy because the indications on the product label are incorrect.

    Product
    COLOSTAT — COLOSTAT (RHAMNUS PURSHIANA, SPIGELIA ANTHELMIA, TARAXACUM OFFICINALE, CAJUPUTUM, HYDRASTIS CANADENSIS, ALUMINA, CINA, CINCHONA OFFICINALIS, LYCOPODIUM CLAVATUM, MAGNESIA PHOSPHORICA, MANDRAGORA OFFICINARUM, NUX VOMICA)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E018000·2020-03-31

    Cummins Recalls B6.7 Diesel Engines Due to Fuel Heater Fire Risk

    Cummins is recalling specific B6.7 diesel engines used in school buses, trucks, and emergency vehicles because the fuel heater may overheat, melt, or cause a fire.

    Product
    FUEL SYSTEM, DIESEL: PRE-HEATER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V189000·2020-03-31

    Subaru Recalls 2019 Crosstrek Vehicles for Rear Seat Belt Defect

    Subaru is recalling 2019 Crosstrek vehicles because the rear seat belt locking mechanism may not function as intended, increasing injury risk in crashes.

    Product
    SUBARU — SUBARU CROSSTREK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V188000·2020-03-30

    Nissan Recalls NV, Titan, Armada, QX56 for Air Bag Inflator Defect

    Nissan is recalling 216,678 vehicles from 2011-2017 because the driver-side air bag inflator may rupture during deployment, potentially causing serious injury or death.

    Product
    INFINITI — INFINITI, NISSAN QX56, NV, ARMADA, TITAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V186000·2020-03-27

    Can-Am Recalls 2020 Spyder RT Motorcycles Due to Brake Failure Risk

    Bombardier is recalling 2020 Can-Am Spyder RT motorcycles because a brake support could break during emergency braking, causing total loss of braking ability.

    Product
    CAN-AM — CAN-AM SPYDER RT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V185000·2020-03-26

    BMW Recalls 328d Vehicles for Driveline Joint Defect

    BMW is recalling 2013-2016 328d xDrive vehicles because a driveline joint may fail, causing loss of rear power and increasing crash risk.

    Product
    BMW — BMW 328D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V183000·2020-03-26

    Chrysler Recalls 2019 Jeep Grand Cherokee and Dodge Durango for Driveline Defect

    Chrysler is recalling 2019 Jeep Grand Cherokee and Dodge Durango vehicles because insufficiently hardened front differential pinion gears can wear down, leading to a loss of power or the PARK function.

    Product
    JEEP — JEEP, DODGE GRAND CHEROKEE, DURANGO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E017000·2020-03-26

    Land Rover Recalls 2020 Range Rover Evoque Headliners for Safety Defect

    Land Rover is recalling 2020 Range Rover Evoque vehicles because some headliners lack a required metal plate, potentially reducing head impact protection in a crash.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V180000·2020-03-26

    2019 Mercedes-Benz and Freightliner Sprinter Recall for Manual Error

    Daimler Vans USA is recalling 2019 Sprinter vans because the Operator's Manual may contain incorrect information about the automatic parking function, potentially increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 1500, SPRINTER 2500, SPRINTER 3500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V184000·2020-03-26

    GM Recalls 2019-2020 Chevrolet Bolt EV for Rear Door Cable Defect

    General Motors is recalling 2019-2020 Chevrolet Bolt EVs because a rear door cable may be too long, potentially causing the door to open unintentionally while driving.

    Product
    CHEVROLET — CHEVROLET BOLT EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1499-2020·2020-03-25

    Philips Recalls HeartStart MRx Defibrillators Due to Internal Damage Risk

    Philips is recalling HeartStart MRx Monitor/Defibrillators because internal damage from drops or shocks may prevent therapy delivery, even if the device appears undamaged.

    Product
    HeartStart MRx Monitor/Defibrillators with model numbers M3535A M3536A, M3536M, M3536MC, M3536M2, M3536M3, M3536M4, M3536M5, M3536M6, M3536M7, M3536M8, and M3536M9.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0860-2020·2020-03-25

    Chicago Indoor Garden Recalls Sprout Salad Due to E. coli Outbreak

    Chicago Indoor Garden, Inc. is recalling Sprout Salad 6 oz. because FDA analysis found E. coli and linked the product to an outbreak.

    Product
    Sprout Salad 6 oz. Product contains red clover sprouts.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0861-2020·2020-03-25

    Chicago Indoor Garden Recalls Mixed Greens Contaminated with E. coli

    Chicago Indoor Garden is recalling Mixed Greens containing red clover sprouts because FDA testing found E. coli. The product was distributed nationwide, primarily through Whole Foods.

    Product
    Mixed Greens 4 oz. Product contains red clover sprouts.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0858-2020·2020-03-25

    Chicago Indoor Garden Recalls Red Clover Products Due to E. coli

    Chicago Indoor Garden, Inc. is recalling Red Clover products because FDA analysis found E. coli and linked the firm to an outbreak.

    Product
    Red Clover 4 oz, Red Clover 2 Lbs. Products have Red Clover as an ingredient.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1036-2020·2020-03-25

    UP2 Libido Supplement Recalled for Undeclared Sildenafil

    Med Man Distribution is recalling UP2 dietary supplements because FDA analysis found undeclared sildenafil, a prescription drug, in the product.

    Product
    UP2, Dietary Supplement, All Natural Libido for Men & Women, a) one pack, b) four pack, c) ten pack capsules per carton, Exclusively Manufactured and Formulated by: Buy Wise Marketing, 4234 I-75 Business Spur, Sault Ste Marie, MI 49783, Ultimatepleasure2.com.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0859-2020·2020-03-25

    Chicago Indoor Garden Recalls Spring Salad Sprouts Due to E. coli

    Chicago Indoor Garden, Inc. is recalling Spring Salad 6 oz. containing red clover sprouts because FDA testing found E. coli and linked the product to an outbreak.

    Product
    Spring Salad 6 oz. Product contains red clover sprouts.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1015-2020·2020-03-25

    Perrigo Recalls Ranitidine Tablets Due to Possible N-Nitrosodimethylamine Contamination

    Perrigo Company PLC is recalling specific lots of Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, due to a CGMP deviation and possible contamination with the impurity N-nitrosodimethylamine.

    Product
    Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 150 tablets per bottle. [NDC: Brand] NDC H.E.B.: 37808-876-47; NDC Equate: 49035-876-47
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1474-2020·2020-03-25

    CME America BodyGuard Infusion Pump Systems Recalled for Delivery Inaccuracy

    CME America is recalling BodyGuard Infusion Pump Systems because they may deliver drugs at inaccurate rates, potentially causing faster or slower than expected medication administration.

    Product
    CME America BodyGuard Infusion Pump System, All models of BG 323, BG 121, BG 545, BG CV545, BG 575, BG CV575, and CMExpress
    Category
    Medical Device
    Distribution
    45 states
  • SevereFDA (Drugs)·D-1012-2020·2020-03-25

    Perrigo Recalls Ranitidine Tablets Due to Potential N-Nitrosodimethylamine Contamination

    Perrigo Company PLC is recalling Regular Strength Acid Reducer (Ranitidine) tablets due to a CGMP deviation and possible contamination with the impurity N-nitrosodimethylamine.

    Product
    Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 30 tablets per bottle. [NDC: Brand] NDC CVS Health: 69842-293-65; NDC Equaline 41163-931-65; NDC Family Wellness: 55319-876-65; NDC Good Sense 0113-0876-65; NDC H.E.B.: 37808-876-65; NDC Harris Teeter: 69256-876-65…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1020-2020·2020-03-25

    Perrigo Recalls Ranitidine Tablets Due to Potential N-Nitrosodimethylamine Contamination

    Perrigo Company PLC is recalling specific lots of Maximum Strength Acid Reducer, Cool Mint Ranitidine tablets due to a CGMP deviation and possible contamination with the impurity N-nitrosodimethylamine.

    Product
    Maximum Strength Acid Reducer, Cool Mint Ranitidine tablets, USP 150 mg, 40 tablets per bottle. [Brand, NDC] NDC Up & Up: 11673-950-58
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1037-2020·2020-03-25

    Bow and Arrow Libido Supplement Recalled for Undeclared Sildenafil

    Med Man Distribution is recalling Bow & Arrow dietary supplements because they contain undeclared sildenafil, a prescription drug ingredient not listed on the label.

    Product
    Bow & Arrow, Dietary Supplement, Libido Enhancer for Men, a) Four pack, b) Ten pack capsules per carton, Exclusively Manufactured by: Medicine Man Distribution, 4234 I-75 Business Spur, Sault Ste Marie, MI 49783
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1023-2020·2020-03-25

    Perrigo Recalls Ranitidine Tablets Due to Possible N-Nitrosodimethylamine Contamination

    Perrigo Company PLC is recalling Maximum Strength Acid Reducer, Cool Mint Ranitidine tablets due to a CGMP deviation and possible contamination with the impurity N-nitrosodimethylamine.

    Product
    Maximum Strength Acid Reducer, Cool Mint Ranitidine tablets, USP 150 mg, 65 tablets per bottle. [Brand, NDC] NDC Basic Care: 0113-7950-09; NDC CVS Health: 59779-950-09; NDC Equate: 49035-800-09; NDC Good Neighbor Pharmacy: 46122-533-09; NDC Kroger: 30142-891-09; NDC Topcare…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V181000·2020-03-25

    2019 Freightliner and Mercedes-Benz Sprinter Brake Hose Recall

    Daimler Vans USA is recalling 2019 Freightliner and Mercedes-Benz Sprinter vans because a fender liner may chafe the brake hose, risking brake fluid loss and increased stopping distance.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 1500, SPRINTER 4500, SPRINTER (VS30)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1025-2020·2020-03-25

    Perrigo Recalls Ranitidine Tablets Due to Potential N-Nitrosodimethylamine Contamination

    Perrigo Company PLC is recalling Maximum Strength Acid Reducer, Cool Mint Ranitidine tablets due to a CGMP deviation and possible contamination with the impurity N-nitrosodimethylamine.

    Product
    Maximum Strength Acid Reducer, Cool Mint Ranitidine tablets, USP 150 mg, 90 tablets per bottle. [Brand, NDC] NDC Equate: 49035-800-75; NDC Up & Up: 11673-950-75
    Category
    Drug
    Distribution
    Distributed nationwide