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.

48901–48925 of 78743

  • ModerateFDA (Devices)·Z-0664-2017·2016-12-07

    Merge FlexConnect Software Recalled for Data Processing Errors

    Merge Healthcare is recalling Merge FlexConnect software version 1.0 because communication protocols were not properly handled, preventing data from being processed by the LIS software.

    Product
    Merge FlexConnect software, a component of Merge LIS. Merge FlexConnect is middleware used in conjunction with Merge LIS to facilitate connection to external applications
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0155-2017·2016-12-07

    Burel Recalls Hyolev MB Urinary Antiseptic Tablets Due to Manufacturing Deficiencies

    Burel Pharmaceuticals is recalling 2,861 bottles of Hyolev MB Urinary Antiseptic Tablets due to manufacturing deviations that may cause assay or content uniformity failures.

    Product
    Hyolev MB URINARY ANTISEPTIC Tablets, Each tablet for oral administration contains: Hyoscyamine Sulfate 0.12 mg, Methenamine 81 mg, Methylene Blue 10.8 mg, Phenyl Salicylate 32.4 mg, Sodium Phosphate Monobasic 40.8 mg, 90 count bottles, Rx only, Manufactured for: BUREL…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0158-2017·2016-12-07

    Burel Pharmaceuticals Recalls UROPHEN MB Urinary Antiseptic Tablets

    Burel Pharmaceuticals is recalling UROPHEN MB Urinary Antiseptic Tablets due to manufacturing deviations that may cause assay or content uniformity failures.

    Product
    UROPHEN MB URINARY ANTISEPTIC Tablets, Each tablet contains: Methenamine 81.6 mg, Benzoic Acid 9.0 mg, Phenyl Salicylate 36 mg, Methylene Blue 10.8 mg, Hyoscyamine Sulfate 0.12 mg, 100 count bottles, Rx only, Manufactured for: BUREL PHARMACEUTICALS, Richland, MS --- NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0157-2017·2016-12-07

    Burel Pharmaceuticals Recalls Uramit MB Urinary Antiseptic Capsules

    Burel Pharmaceuticals is recalling Uramit MB Urinary Antiseptic Capsules due to manufacturing deviations that may cause assay or content uniformity failures.

    Product
    URAMIT MB URINARY ANTISEPTIC Capsules, Each capsule contains: Methenamine 118 mg, Monobasic Sodium Phosphate 40.8 mg, Phenyl Salicylate 36 mg, Methylene Blue 10 mg, Hyoscyamine Sulfate, 0.12 mg, 100 count bottles, Rx only, Manufactured for: BUREL PHARMACEUTICALS, Richland, MS…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0675-2017·2016-12-07

    Teleflex Recalls Arrow OnControl Bone Marrow Biopsy System Trays

    Teleflex Medical is recalling 113,647 units of Arrow OnControl Bone Marrow Biopsy System Trays due to a potential incomplete seal on the outer sterile package.

    Product
    ARROW OnControl Bone Marrow Biopsy System Tray, Sterile, Rx only, Manufactured for: Teleflex Medical, The Arrow OnControl Bone Marrow Aspiration System is intended for bone marrow aspiration of the iliac crest of adult and pediatric patients. The Arrow¿ OnControl Bone Marrow…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0168-2017·2016-12-07

    Nationwide Laboratories Recalls Phenazopyridine Hydrochloride Tablets Due to CGMP Deviations

    Nationwide Laboratories LLC is recalling Phenazopyridine Hydrochloride Tablets, 200 mg, due to manufacturing deviations that may result in assay or content uniformity failures.

    Product
    Phenazopyridine Hydrochloride Tablets, USP, 200 mg, 100 count bottles, Rx only, Manufactured for: Nationwide Laboratories LLC, Iselin, New Jersey 08830, NDC 42937-702-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0161-2017·2016-12-07

    Burel Pharmaceuticals Recalls Phenazopyridine Hydrochloride Tablets Due to CGMP Deviations

    Burel Pharmaceuticals is recalling 17,788 bottles of Phenazopyridine Hydrochloride Tablets due to manufacturing deviations that may cause assay or content uniformity failures.

    Product
    Phenazopyridine Hydrochloride Tablets, USP, 100 mg, 100 count bottles, Rx only, Manufactured for: Burel Pharmaceuticals, Inc., Richland, MS --- NDC 35573-304-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0670-2017·2016-12-07

    Baxter Recalls Sigma Spectrum Infusion Pumps Due to Speaker Failure Risk

    Baxter Healthcare is recalling 5,976 Sigma Spectrum Infusion Pumps because some speakers may fail prematurely, potentially affecting audible alarms.

    Product
    sigma spectrum VOLUMETRIC INFUSION PUMP with Master Drug Library, V6 Spectrum Infusion Pump, Product Code 35700BAX and 35700BAXR, Unique Device Identifier GTIN 00085412091570, Rx ONLY -- Sigma, LLC Medina, NY 14103 --- NOTE: The speakers are a part of the rear case assembly…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0160-2017·2016-12-07

    Burel Pharmaceuticals Recalls Indiomin MB Capsules Due to Manufacturing Deficiencies

    Burel Pharmaceuticals is recalling 795 bottles of Indiomin MB capsules due to manufacturing deviations that may cause assay or content uniformity failures.

    Product
    Indiomin MB URINARY ANTISEPTIC, ANTISPASMODIC Capsules, Each capsule contains: Methenamine 120 mg, Monobasic Sodium Phosphate 40.8 mg, Methylene Blue, 10 mg; Hyoscyamine Sulfate, 0.12 mg, 100 count, Rx only, Manufactured for: BUREL PHARMACEUTICALS, NDC 35573-315-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E091000·2016-12-06

    Tesla Recalls Universal Mobile Connector Adapters Due to Fire Risk

    Tesla is recalling specific Universal Mobile Connector Adapters because insufficient welds may cause overheating or arcing, increasing the risk of a fire.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:CHARGING:CABLE/CORD:ACCESSORY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V877000·2016-12-06

    Indian Recalls 2014-2017 Motorcycles Due to Fuel Rail Leak Risk

    Indian Motorcycle is recalling 2014-2017 models because the fuel rail may contact other components, causing a fuel leak that increases fire risk.

    Product
    INDIAN — INDIAN CHIEF CLASSIC, ROADMASTER, SPRINGFIELD, CHIEF DARK HORSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17044·2016-12-06

    Atrium Recalls SafeHarbor Vinyl Impact Windows Due to Injury Hazard

    Atrium is recalling about 580 SafeHarbor vinyl impact windows because the glass can separate from the frame during hurricanes, posing an impact injury hazard.

    Product
    SafeHarbor vinyl impact windows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17045·2016-12-06

    Target Recalls Acrylic Hanukkah Menorahs Due to Fire Hazard

    Target is recalling clear acrylic Hanukkah menorahs that can melt when candles are burning, posing a fire hazard. Consumers should stop using the products and return them for a refund.

    Product
    Menorahs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V874000·2016-12-05

    Ford Recalls 2017 Fusion Vehicles for Rear Seat Back Weld Defect

    Ford is recalling 2017 Fusion vehicles because improperly welded left rear seat back pivot pins may fail in a crash, allowing luggage to move into the passenger compartment.

    Product
    FORD — FORD FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E089000·2016-12-05

    Hickory Springs Recalls Phantomizer 19 Inch Conversion Van Seats

    Hickory Springs is recalling specific Phantomizer 19-inch conversion van seats because the slide tracks may not engage properly, increasing injury risk in a crash.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V875000·2016-12-05

    Ford Recalls 2013-2016 Fusion and 2013-2015 Lincoln MKZ for Seat Belt Defect

    Ford is recalling specific 2013-2016 Fusion and 2013-2015 Lincoln MKZ vehicles because heat from seat belt pretensioners may cause anchor cables to fail, increasing injury risk in a crash.

    Product
    FORD — FORD, LINCOLN FUSION, MKZ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V872000·2016-12-05

    Peterbilt Trucks Recalled for Brake Light Switch Defect

    PACCAR is recalling 2017 Peterbilt trucks because brake lights may not illuminate when brakes are applied, increasing crash risk.

    Product
    PETERBILT — PETERBILT 330, 365, 386, 325
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V873000·2016-12-05

    Entegra Recalls 2017 Cornerstone Vans Due to Collision System Defect

    Entegra is recalling 125 2017 Cornerstone vehicles because the collision mitigation system may be installed upside down, reducing its functionality and increasing crash risk.

    Product
    ENTEGRA — ENTEGRA CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·115-2016 EXP·2016-12-04

    National Steak and Poultry Recalls Undercooked Ready-to-Eat Chicken Products

    National Steak and Poultry is recalling approximately 1.99 million pounds of ready-to-eat chicken products due to possible undercooking, which may allow bacterial pathogens to survive.

    Product
    National Steak Processors (2024), LLC. — National Steak and Poultry Recalls Ready-To-Eat Chicken That May Be Undercooked
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V870000·2016-12-02

    GM Recalls 2017 Chevrolet Malibu for Rear Side Air Bag Defect

    General Motors is recalling 2017 Chevrolet Malibus because the right-hand rear side air bag inflator manifold may have insufficient welds, posing a risk of debris or failure during a crash.

    Product
    CHEVROLET — CHEVROLET MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V866000·2016-12-02

    Forest River Recalls 2017 Puma Trailers for Incorrect Federal Tire Placards

    Forest River is recalling 2017 Puma trailers because incorrect Federal placards list wrong tire and rim information, which could lead to under-inflation and increased crash risk.

    Product
    FOREST RIVER — FOREST RIVER PUMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V869000·2016-12-02

    Thor Motor Coach Recalls 2017 Quantum RQ29 Motorhomes for Missing Light

    Thor Motor Coach is recalling 32 model year 2017 Quantum RQ29 motorhomes because they may be missing a required mid-ship marker light, which can increase crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH QUANTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V867000·2016-12-02

    Mitsubishi Recalls Outlander Sport Vehicles for Lift Gate Corrosion Risk

    Mitsubishi is recalling 2011-2012 and 2016 Outlander Sport vehicles because the lift gate support tube may corrode, causing the gate to fall suddenly and increase injury risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide