The Recall Desk

State

Utah product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49401–49425 of 78743

  • ModerateFDA (Devices)·Z-0299-2017·2016-11-02

    Keystone Dental PrimaConnex Straight Implant Recall Due to Cover Screw Mismatch

    Keystone Dental Inc. is recalling 55 units of PrimaConnex Straight Implants because small diameter cover screws were packaged with regular diameter implants.

    Product
    Keystone Dental PrimaConnex¿ Straight Implant TC, RD Internal Connection 4.0 x 11.5mm. Product code:15613K Implants are intended for use in partially or fully edentulous mandibles and maxillae, in support of single or multiple-unit restorations includ-ing; cement retained…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0298-2017·2016-11-02

    TZ Medical Recalls Mis-Labeled Neptune Plus Hemostatic Pads

    TZ Medical is recalling Neptune Plus hemostatic pads because the labels incorrectly state they include an antimicrobial barrier.

    Product
    Neptune Plus (Hemostatic Pad), Part Numbers: 8870-03 Neptune Pad is used to promote the rapid control of bleeding and provide hemostasis for lacerations, abrasions, vascular access sites and following surgical incision. It can be used to achieve hemostasis at the skin surface…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0319-2017·2016-11-02

    Siemens CMV IgM Assay Recalled for Increased Imprecision

    Siemens Healthcare Diagnostics is recalling IMMULITE CMV IgM Assay kits due to reported increases in imprecision and high coefficient of variation (CV) values.

    Product
    IMMULITE/ IMMULITE 1000 Systems CMM CMV IgM Assay, REF/Catalog Number LKCM1(D) - 100 tests (US), Siemens Material Number (SMN) 10370301 (US), Unique Device Identification Number (UDI) 00630414985718 (US); and REF/Catalog Number LKCM1 - 100 tests (OUS); SMN 10381296 (OUS), UDI…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0281-2017·2016-11-02

    Bob's Red Mill Guar Gum Recalled for Misidentified Ingredient

    Bob's Red Mill is voluntarily recalling one lot of Guar Gum due to the inclusion of a misidentified ingredient, hydroxyethylcellulose.

    Product
    Label reads in part "*** Bob's Red Mill *** PREMIUM GUAR GUM SUPERB GLUTEN FREE THICKENER & BINDER *** NET WT 8 OZ ***" Product is packaged in multilayered flexible film with multiple colors. Firm brand name is printed in red. Case contains 8/8 oz. packages. UPC 0…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0356-2017·2016-11-02

    Wilton Black Airbrush Color Recalled for Mold, Yeast, or Bacteria

    Wilton Brands is recalling 16,446 bottles of Black Airbrush Color found to contain mold, yeast, or bacteria. The product was distributed nationwide in the U.S. and Canada.

    Product
    Wilton Black Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0115-2017·2016-11-02

    Invokamet Recalled for Incorrect or Missing Package Insert Labeling

    Janssen Ortho L.L.C. is recalling Invokamet tablets because Xarelto prescribing information outserts may be affixed to the bottles instead of the correct Invokamet inserts.

    Product
    INVOKAMET — INVOKAMET (CANAGLIFLOZIN AND METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0313-2017·2016-11-02

    Ortho-Clinical Diagnostics Recalls VITROS HBsAg Controls Due to Performance Drift

    Ortho-Clinical Diagnostics is recalling VITROS HBsAg Controls because signal/cutoff results may increase during the 5-day reconstituted timeframe, potentially affecting performance monitoring.

    Product
    VITROS Immunodiagnostic Products HBsAg Controls, Product Code 6800598 For in vitro diagnostic use only. For use in monitoring the performance of the VITROS ECi/ECiQ Immunodiagnostic Systems, the VITROS 3600 Immunodiagnostic System and the VITROS 5600 Integrated System when…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E082000·2016-11-01

    Omix Ada Recalls Replacement Steering Sector Shafts for Early Jeeps

    Omix Ada is recalling 344 replacement steering sector shafts for early Willys and Jeep vehicles due to incomplete heat treatment that may cause premature failure.

    Product
    STEERING:GEAR BOX:SHAFT SECTOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V795000·2016-11-01

    Spartan Motors Recalls Transit Bus Chassis Cabs Due to Exhaust Fire Risk

    Spartan Motors is recalling 245 model year 2011-2017 Transit Bus Chassis Cabs because a disconnecting exhaust tube may expose the floor to high heat, increasing fire risk.

    Product
    SPARTAN MOTORS — SPARTAN MOTORS TRANSIT BUS CHASSIS CAB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17023·2016-11-01

    Kikkerland Teapots with Bamboo Stands Recalled for Fire Hazard

    Kikkerland Design is recalling teapots with bamboo stands because the stands can catch fire. No injuries have been reported.

    Product
    Kikkerland and Cost Plus World Market brand teapots with bamboo stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V792000·2016-10-31

    Mitsubishi Recalls Outlander Sport Vehicles for Wiper Motor Corrosion Risk

    Mitsubishi is recalling 2011-2015 Outlander Sport vehicles because water leaks can corrode the wiper motor, potentially causing loss of visibility and increasing crash risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V791000·2016-10-31

    Mitsubishi Recalls Outlander Vehicles for Wiper Link Corrosion Risk

    Mitsubishi is recalling 2007-2013 Outlander vehicles because water intrusion can corrode the wiper link, potentially causing the wipers to stop working and reducing visibility.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V788000·2016-10-28

    Mazda Recalls 2010-2011 Tribute Vehicles for Fuel Leak Risk

    Mazda is recalling 2010-2011 Tribute vehicles because a cracked fuel delivery module may leak fuel, increasing the risk of fire.

    Product
    MAZDA — MAZDA TRIBUTE, TRIBUTE HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E081000·2016-10-28

    Vega Motorcycle Helmets Recalled for Failing Federal Safety Standards

    Vega Helmet Corporation is recalling specific XTA and XTA Touring half helmets because they may not adequately protect the wearer's head in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V787000·2016-10-28

    Forest River Recalls 2017 Salem and Wildwood Trailers for Labeling Errors

    Forest River is recalling 92 model year 2017 Salem and Wildwood recreational trailers because the Federal Placard Label and VIN incorrectly state the vehicles have two axles instead of one.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V786000·2016-10-28

    Starcraft RV Recalls 2017 AR-ONE Trailers for Incorrect Load Labels

    Starcraft RV is recalling 94 model year 2017 AR-ONE trailers because incorrect Federal Placard and Cargo Carrying Capacity labels may lead to overloading and increased crash risk.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT AR-ONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V784000·2016-10-27

    Holiday Rambler Vacationer Motorhomes Recalled for Front Truss Support Defect

    REV Recreation Group is recalling 2015-2016 Holiday Rambler Vacationer motorhomes because a front truss may not be adequately supported, risking wire or hydraulic line damage.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER VACATIONER
    Category
    Vehicle
    Distribution
    Distributed nationwide