The Recall Desk

State

Utah product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41976–42000 of 78733

  • ModerateFDA (Devices)·Z-1276-2018·2018-04-11

    Phadia Prime software recall for EliA assay retesting function

    Phadia Ab is recalling Phadia Prime software versions up to 2.1.4 to prevent the use of the 'OK to All' function when rejecting and retesting EliA assay samples.

    Product
    Phadia Prime software, article number 12-4101-00, as used in combination with the Phadia 250 Instrument, article number 12-3900-01 and EliA Assays. This recall is for any Phadia Prime software version up to and including the current version, 2.1.4.
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Devices)·Z-1286-2018·2018-04-11

    Arrow Radial Artery Catheterization Kits Recalled for Shelf Life Labeling

    Arrow International is recalling Radial Artery Catheterization Kits because the included povidone iodine prep pads do not meet the 36-month shelf life requirement and should be labeled with a 24-month shelf life.

    Product
    Radial Artery Catheterization Kit; Model: AK-04220
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1287-2018·2018-04-11

    Arrow Arterial Access Tray Recall for Povidone Iodine Shelf Life Labeling

    Arrow International is recalling Arterial Access Trays because the included povidone iodine prep pads do not meet the 36-month shelf life requirement and must be labeled with a 24-month shelf life.

    Product
    Arterial Access Tray, introducer catheter; Model: GU-04020
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1313-2018·2018-04-11

    Phadia Recalls ImmunoCAP Allergen c6 Amoxicilloyl Due to Stability Failures

    Phadia US Inc is recalling 950 units of ImmunoCAP Allergen c6, Amoxicilloyl because the product failed to meet stability specifications.

    Product
    ImmunoCAP Allergen c6, Amoxicilloyl ( Article number 14-4451-016). ImmunoCAP Specific IgE is an in vitro quantitative assay for the measurement of allergen specific IgE in human serum or plasma; to be used with the instrument Phadia 250, Phadia 1000, Phadia 2500 and Phadia…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1285-2018·2018-04-11

    Arrow Radial Artery Catheterization Kits Recalled for Shelf Life Labeling Error

    Arrow International is recalling 570 Radial Artery Catheterization Kits because the included povidone iodine prep pads are labeled with an incorrect 36-month shelf life.

    Product
    Radial Artery Catheterization Kit; Model: AK-04122
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·032-2018·2018-04-11

    Koch Foods Recalls Beef Patties Due to Plastic Contamination

    Koch Foods is recalling approximately 119,480 pounds of beef rib-shaped patties that may contain thin blue plastic pieces. No adverse reactions have been reported.

    Product
    Koch Foods — Koch Foods Inc. Recalls Beef Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1312-2018·2018-04-11

    Phadia Recalls ImmunoCAP Allergen c5 Ampicilloyl Test Kits

    Phadia US Inc is recalling ImmunoCAP Allergen c5, Ampicilloyl test kits because stability specifications were not met.

    Product
    ImmunoCAP Allergen c5, Ampicilloyl (article number 14-4450-01). ImmunoCAP Specific IgE is an in vitro quantitative assay for the measurement of allergen specific IgE in human serum or plasma. To be used with the instrument Phadia 250, Phadia 1000, Phadia 2500 and Phadia…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0618-2018·2018-04-11

    InvaGen Recalls Bupropion Hydrochloride Tablets for Dissolution Failures

    InvaGen Pharmaceuticals is recalling specific lots of Bupropion Hydrochloride Extended-Release Tablets because they failed dissolution specifications during stability testing.

    Product
    BUPROPION HYDROCHLORIDE (SR) — BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0619-2018·2018-04-11

    InvaGen Recalls Bupropion Hydrochloride Tablets for Dissolution Failures

    InvaGen Pharmaceuticals is recalling specific lots of Bupropion Hydrochloride Extended-Release Tablets because they failed dissolution specifications during stability testing.

    Product
    BUPROPION HYDROCHLORIDE (SR) — BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V226000·2018-04-10

    Keystone Recalls 2018 Raptor and Carbon Trailers for Fuel Fire Risk

    Keystone is recalling 2018 Raptor and Carbon fifth-wheel trailers because missing fuel barriers allow absorption into the floor, increasing fire risk.

    Product
    KEYSTONE — KEYSTONE RAPTOR, CARBON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18735·2018-04-10

    2017 Can-Am Outlander ATVs Recalled for Steering Shaft Crash Hazard

    BRP is recalling 2017 Can-Am Outlander and Outlander Max ATVs because the dynamic power steering shaft can break, causing a loss of steering control and crash hazard.

    Product
    2017 Can-Am Outlander and Outlander Max All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V228000·2018-04-10

    Indian Motorcycle Recalls 2018 Models Due to Unintended Starting Risk

    Indian Motorcycle is recalling 3,341 2018 models because corrosion in the combination switch may cause the bike to start unintentionally, posing a carbon monoxide risk.

    Product
    INDIAN — INDIAN SPRINGFIELD DARK HORSE, CHIEF, CHIEF VINTAGE, CHIEFTAIN ELITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V225000·2018-04-09

    MCI Recalls 2018 J4500 Motor Coaches Due to Window Separation Risk

    Motor Coach Industries is recalling 2018 MCI J4500 motor coaches because the rear left window may separate, creating a road hazard and increasing crash risk.

    Product
    MCI — MCI J4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V223000·2018-04-09

    MCI Recalls 2018 J4500 Coaches Due to Taillight Wiring Defect

    Motor Coach Industries is recalling 2018 J4500 vehicles because a wiring harness may contact the coolant tank, causing the left taillight to fail and reducing visibility.

    Product
    MCI — MCI J4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E022000·2018-04-06

    Keystone Recalls Husky Fifth Wheel Trailer Hitches Due to Fastener Loosening

    Keystone is recalling specific Husky fifth wheel trailer hitches because fasteners may loosen, potentially causing the jaws to open unexpectedly and increasing crash risk.

    Product
    TRAILER HITCHES:FIFTH WHEEL ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V222000·2018-04-06

    Forest River Surveyor Recalled for Incorrect Federal Tire Placard Information

    Forest River is recalling 2018 Surveyor recreational trailers because the Federal Placard lists incorrect tire sizes and pressures, which could lead to over-inflation and increased crash risk.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E018000·2018-04-05

    Brembo Motorcycle Front Brake Master Cylinders Recalled for Piston Cracking

    Brembo is recalling specific motorcycle front brake master cylinders because the internal piston may crack and fail, potentially causing a loss of front braking ability.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:MASTER CYLINDER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V219000·2018-04-05

    Newmar Recalls 2018-2019 New Aire Motorhomes Due to Valve Stem Defect

    Newmar is recalling 2018-2019 New Aire motorhomes because a wheel valve stem stabilizer may dislodge, potentially causing tire damage and increasing crash risk.

    Product
    NEWMAR — NEWMAR NEW AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V221000·2018-04-05

    Honda Recalls 2018 Pilot, Ridgeline, and Acura MDX for Seat Rivet Defect

    Honda is recalling 2018 Pilot, Ridgeline, and Acura MDX vehicles because improperly manufactured seat rivets may break in a crash, increasing injury risk.

    Product
    HONDA — HONDA, ACURA RIDGELINE, PILOT, MDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V220000·2018-04-05

    Mitsubishi Recalls 2004-2006 Lancers for Air Bag Inflator Defect

    Mitsubishi is recalling 2004-2006 Lancers because passenger air bag inflators may explode during deployment, potentially causing serious injury or death.

    Product
    MITSUBISHI — MITSUBISHI LANCER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V218000·2018-04-05

    Doepker Recalls 2015-2016 Flatdeck Semi Trailers Due to Frame Cracking

    Doepker is recalling 2015-2016 53-foot Tridem Galvanized Highboy Flatdeck Semi trailers because lower rail main beam flanges may crack, potentially causing loads to shift and spill onto the road.

    Product
    DOEPKER — DOEPKER HG FLATDECK SEMI
    Category
    Vehicle
    Distribution
    Distributed nationwide