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.

47251–47275 of 78743

  • SevereFDA (Food)·F-1665-2017·2017-03-29

    Lakeview Cheese Recalls Pepper Jack and Jalapeno Products for Listeria Risk

    Lakeview Cheese Co. is recalling specific pepper jack and jalapeno cheese products due to potential Listeria monocytogenes contamination.

    Product
    Food City random weight cut Pepper Jack Cheese., Also sold as Banquet Baby Jalap Jk RW Wheel 18/2#; Banquet Wheel Jalapeno Jk LH 3# wheel exact weight.; LH Pepper Jack 4/13# Lakeview brand. Longhorn identifies the shape of the cheese. Banquet is a Lakeview brand name.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1520-2017·2017-03-29

    CareFusion Alaris System PC Unit Recall for Battery Alarm Failure

    CareFusion is recalling Alaris System PC units because low battery alarms may fail to trigger before the battery discharges, stopping all infusion channels.

    Product
    Alaris System PC unit, model no. 8000 and 8015. The central programming, monitoring and power supply component for the Alaris infusion pump System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1498-2017·2017-03-29

    Merge Eye Station Import Utility Recalled for System Lockup Risk

    Merge Healthcare is recalling the Eye Station Import Utility software because system lockups may cause patient injury or delay diagnosis.

    Product
    Merge Eye Station Import Utility (ESIU). The firm name on the labeling is Merge Healthcare.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1517-2017·2017-03-29

    Merge Healthcare Recalls Merge Cardio Software Due to Data Integrity Issues

    Merge Healthcare is recalling Merge Cardio software versions 9.0 through 9.0.8 because users can merge device files with confirmed reports, potentially adding unverified information.

    Product
    Merge Cardio software. Product Usage: Merge Cardio is a system intended to be used to acquire, store, print, transfer, and archive clinical information including images, Hemodynamic studies and reports, measurements (via import from DICOM Structured Reporting, text files…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1627-2017·2017-03-29

    Diamond Crystal Cocoa Powder Recalled for Potential Metal Contamination

    Diamond Crystal Brands is recalling Chef's Companion Natural Cocoa Powder because metal pieces were found missing from a sifter screen during sanitation.

    Product
    Natural Cocoa Powder 22-24% cocoa butter, Net Wt. 5 lbs. (2.27 kg) packaged under the following brand name: Chef's Companion: 1 bag /case, UPC 10719098582240; Diamond Crystal Brands, Inc. Savannah, GA 31405
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1499-2017·2017-03-29

    Stanley Security Recalls 500 Arial Wireless Call Pendants

    Stanley Security Solutions is recalling 500 Arial Wireless Water-Resistant Call Pendants because they were incorrectly programmed, which may prevent alarms from sounding when the button is pressed.

    Product
    Arial Wireless Water-Resistant Call Pendant The Arial Pendant tag is part of the Arial wireless emergency call management system. It enables residents in assisted living, skilled nursing or independent living to call staff with the press of a button.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1494-2017·2017-03-29

    Nidek EC-5000 Excimer Laser Software Recall for Unintended Correction Programming

    Nidek Inc is recalling Final Fit Software versions 1.11 and 1.12 for the EC-5000 Excimer Laser System because treatment planning could be programmed with an unintended correction.

    Product
    Final Fit Software Version 1.11 and 1.12; PC Based software installed outside Nidek EC-5000 Excimer Laser System. Ophthalmic laser system use for correction of corneal refraction and ablation of the corneal surface. The system is composed of a laser generator which…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1626-2017·2017-03-29

    Diamond Crystal Cocoa Powder Recalled for Potential Metal Contamination

    Diamond Crystal Brands is recalling specific lots of Natural Cocoa Powder because metal pieces were found missing from a sifter screen during sanitation.

    Product
    Natural Cocoa Powder 10-12% cocoa butter, Net Wt. 5 lbs. (2.27 kg) packaged under the following brand names: Monarch distributed by U.S. Foodservice UPC 50758108102533; Chef's Companion: 1 bag /case, UPC 10719098582233; and 6 bags/case, UPC 50719098582293 Diamond Crystal…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V217000·2017-03-29

    2016 Thomas Built Buses Saf-T-Liner C2 Recalled for Transmission Defect

    Daimler Trucks North America is recalling one 2016 Thomas Built Buses Saf-T-Liner C2 school bus because the transmission grade brake may fail to deactivate, increasing crash risk in slippery conditions.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17120·2017-03-29

    Juratoys Recalls Janod Push Toy Trolleys Due to Impact Injury Hazard

    Juratoys is recalling four models of Bricolo by Janod push toy trolleys because they can tip backwards, posing an impact injury hazard to children.

    Product
    Bricolo by Janod ® Push toy trolleys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1539-2017·2017-03-29

    Integra Recalls Panta Nails Due to Potential Sterility Seal Issues

    Integra LifeSciences is voluntarily recalling Panta and Panta XI Nails because package seals may not maintain intended sterility.

    Product
    Panta Nail, Rx only, Sterile,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1642-2017·2017-03-29

    Manzana Recalls Trader Joe's Apple Sauce Due to Glass Fragments

    Manzana Products Co. is recalling Trader Joe's Organic Unsweetened Apple Sauce after customer complaints and inspections revealed small pieces of glass in the product.

    Product
    Trader Joe's Organic Unsweetened Apple Sauce; 24 oz. glass jar. Best Before date stamped on top of lid. UPC: 00194877 Distributed by Trader Joe's, Monrovia, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1641-2017·2017-03-29

    Manzana Recalls Trader Joe's Apple Sauce Due to Glass Fragments

    Manzana Products Co. is recalling Trader Joe's All Natural Unsweetened Apple Sauce after finding small pieces of glass in the product.

    Product
    Trader Joe's All Natural Unsweetened Apple Sauce; 24 oz. glass jar. Best Before date stamped on top of lid. UPC: 00014359 Distributed by Trader Joe's, Monrovia, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1485-2017·2017-03-29

    PureWick External Catheter Recalled for Latex Labeling Errors

    Purewick Corporation is recalling 176,863 units of the PureWick External Catheter for Women because the labeling failed to disclose the presence of dry natural rubber and incorrectly stated the product was latex-free.

    Product
    PureWick External Catheter for Women-Wick Product Usage: A flexible, contoured external catheter (a Wick) is positioned between the labia and gluteus muscles. The function of the Wick is to draw urine away from the body through the Wick to a storage container away from the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1540-2017·2017-03-29

    Hitachi Oasis MRI System Recalled for Image Data Transfer Errors

    Hitachi Medical Systems America Inc is recalling 210 Hitachi Oasis MRI Systems because image data transferred to workstations showed errors on the slice position reference image.

    Product
    Hitachi Oasis MRI System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1528-2017·2017-03-29

    BioMerieux Recalls ETEST Fosfomycin Strips Due to Unsupported Shelf-Life Claims

    BioMerieux SA is recalling ETEST Fosfomycin FM1024 strips because internal testing does not support the current shelf-life claims.

    Product
    ETEST Fosfomycin FM1024 Blister packaging, Product Name: ETEST Fosfomycin FM 0.064-1024. ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1521-2017·2017-03-29

    BioMerieux Recalls ETEST Ceftazidime Strips Due to Stability Issues

    BioMerieux SA is recalling ETEST Ceftazidime TZ256 strips because their shelf-life claims are not supported by internal testing.

    Product
    ETEST Ceftazidime TZ256 Foam packaging, Product Name: ETEST Ceftazidime TZ 0.016-256. ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas, Staphylococcus…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1541-2017·2017-03-29

    Hitachi Echelon Oval MRI System Recalled for Image Data Errors

    Hitachi Medical Systems America Inc is recalling 25 Hitachi Echelon Oval MRI Systems because image data transferred to workstations showed errors on the slice position reference image.

    Product
    Hitachi Echelon Oval MRI System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1500-2017·2017-03-29

    Haag-Streit EyeSuite Software Recalled for Potential Patient Data Misattribution

    Haag-Streit USA Inc is recalling EyeSuite i.8.2.1.0 software due to a risk that patient data may be stored under the wrong patient on the DICOM Server.

    Product
    EyeSuite i.8.2.1.0 Software for ophthalmic use including selection of Intra Ocular Lenses (IOLs).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1486-2017·2017-03-29

    Merge Healthcare Recalls Cardio Software Due to STAT Study Display Issue

    Merge Healthcare is recalling Merge Cardio software versions 9.0 through 10.1.2 because the study list fails to display STAT studies without a manual refresh.

    Product
    Merge Cardio software.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1542-2017·2017-03-29

    Hitachi Echelon MRI System Recalled for Image Data Transfer Errors

    Hitachi Medical Systems America Inc is recalling 68 Hitachi Echelon MRI Systems because image data transferred to workstations showed errors on the slice position reference image.

    Product
    Hitachi Echelon MRI System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1533-2017·2017-03-29

    Siemens Syngo.plaza PACS Systems Recalled for Software Update Issues

    Siemens Medical Solutions is recalling 13 Syngo.plaza PACS systems nationwide due to software update issues. The recall is voluntary and has been terminated.

    Product
    Syngo.plaza, Picture Archiving and Communications System (PACS) Syngo.plaza is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images. It supports the physician in…
    Category
    Medical Device
    Distribution
    Distributed nationwide