State

Utah product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38101–38125 of 78725

LowFDA (Devices)·Z-0691-2019·2019-01-09
R&D Systems Recalls Human sTfR ELISA Kits Due to Incorrect Control Card
R&D Systems is recalling 198 Human sTfR ELISA kits because they were packed with the wrong control data card number.
Product
Quantikine¿ IVD¿ ELISA, Human sTfR Immunoassay kit. Product Usage: The QuantikineTM IVDTM sTFR Enzyme linked immunosorbent assay is intended for the measurement of sTfR concentration in human serum or plasma as an aid in the diagnosis of iron deficiency anemia, especially…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·19V004000·2019-01-08
Daimler Recalls 2014-2017 Sprinter Vans Due to Air Bag Inflator Defect
Daimler Vans USA is recalling 2014-2017 Freightliner and Mercedes-Benz Sprinter vans because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Product
FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V003000·2019-01-08
Daimler Recalls 2015-2017 Sprinter Vehicles Due to Air Bag Inflator Defect
Daimler Vans USA is recalling 2015-2017 Freightliner and Mercedes-Benz Sprinter 2500 and 3500 vehicles because driver air bag inflators may explode during deployment.
Product
MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 2500, SPRINTER 3500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V027000·2019-01-07
MCI Coaches Recalled for Hydraulic Steering System Locking Risk
Motor Coach Industries is recalling specific 1997-2015 coaches because a steering defect may cause loss of control at highway speeds.
Product
MCI — MCI 102EL3, J4500, E4500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V026000·2019-01-07
Keystone Recalls Dutchmen Travel Trailers Due to Tire Clearance Issue
Keystone RV is recalling 2017-2019 Dutchmen Voltage and 2019 Endurance travel trailers because tires may contact the rear floor support, affecting handling.
Product
DUTCHMEN — DUTCHMEN VOLTAGE, ENDURANCE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V001000·2019-01-07
Ford Recalls Vehicles for Air Bag Inflator Explosion Risk
Ford is recalling specific 2010-2014 models because passenger air bag inflators may explode due to humidity, posing a serious injury risk.
Product
FORD — FORD, LINCOLN, MERCURY MUSTANG, RANGER, EDGE, MKX
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V002000·2019-01-07
Tesla Recalls 2014-2016 Model S Vehicles Due to Air Bag Inflator Defect
Tesla is recalling 2014-2016 Model S vehicles because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Product
TESLA — TESLA MODEL S
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19E004000·2019-01-06
WSB SC101 Motorcycle Helmets Recalled for Impact Protection Failure
WSB Inc is recalling SC101 half-helmets manufactured in January 2018 because they may not adequately protect the wearer's head during an impact.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·19V025000·2019-01-04
Vantage AMS Edge II Recalled for Fuel Leak Fire Risk
Vantage Mobility International is recalling 2014-2017 AMS Edge II vehicles because a deteriorating fuel pump gasket may cause fuel leaks, increasing fire risk.
Product
VANTAGE — VANTAGE AMS EDGE II
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V024000·2019-01-03
Airstream Recalls 2019 Basecamp X Vehicles Due to Incorrect Tire Placard Information
Airstream is recalling 2019 Basecamp X recreational vehicles because the tire placard lists incorrect tire sizes and pressure requirements, which could lead to overinflation and increased crash risk.
Product
AIRSTREAM — AIRSTREAM BASECAMP
Category
Vehicle
Distribution
Distributed nationwide
CriticalNHTSA·19E002000·2019-01-02
Takata Frontal Passenger Air Bag Inflator Recall for 2011 and Newer Vehicles
Takata is recalling certain frontal passenger air bag inflators in 2011 and newer vehicles registered in 22 states and D.C. due to a risk of explosion.
Product
AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0820-2019·2019-01-02
Apio Recalls Eat Smart Salad Shake Ups Due to Listeria
Apio, Inc. is recalling specific varieties of Eat Smart Salad Shake Ups after the Canadian Food Inspection Agency detected Listeria monocytogenes.
Product
Eat Smart Salad Shake Ups - Raspberry Acai/Framboises ET: 5.5 oz. (156 g); US UPC 7 09351-30178 0; Canadian UPC: 7 09351 30196 4. Product of USA Distributed by Apio Inc., Guadalupe, Ca 93434
Category
Food
Distribution
14 states
CriticalNHTSA·19E003000·2019-01-02
Takata Frontal Passenger Air Bag Inflator Recall for 2010+ Vehicles
Takata is recalling specific frontal passenger air bag inflators in 2010 or newer vehicles registered in 22 states due to a risk of explosion.
Product
AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0821-2019·2019-01-02
Apio Recalls Eat Smart Salad Shake Ups Due to Listeria
Apio, Inc. is recalling Eat Smart Salad Shake Ups after the Canadian Food Inspection Agency detected Listeria monocytogenes in the product.
Product
Eat Smart Salad Shake Ups - Sweet Kale/Chou Frise Doux: 5.5 oz. (156 g); US UPC 7 09351-30240 4; Canadian UPC: 7 09351 30243 5. Product of USA Distributed by Apio Inc., Guadalupe, Ca 93434
Category
Food
Distribution
14 states
CriticalNHTSA·19E001000·2019-01-02
Takata Frontal Passenger Air Bag Inflator Recall for Humidity-Related Explosion Risk
Takata is recalling specific frontal passenger air bag inflators that may explode due to humidity and heat, posing a risk of serious injury or death.
Product
AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0819-2019·2019-01-02
Apio Recalls Eat Smart Salad Shake Ups Due to Listeria Risk
Apio, Inc. is recalling Eat Smart Salad Shake Ups in Avocado Ranch flavor because the Canadian Food Inspection Agency detected Listeria monocytogenes in the product.
Product
Eat Smart Salad Shake Ups - Avocado Ranch/Ranch et Avocats: 5.5 oz. (156 g); US UPC: 7 09351-30177 3; Canadian UPC: 7 09351 30195 7; Product of USA Distributed by Apio Inc., Guadalupe, Ca 93434
Category
Food
Distribution
14 states
CriticalFDA (Food)·F-0818-2019·2019-01-02
Apio Recalls Eat Smart Salad Shake Ups Due to Listeria
Apio, Inc. is recalling specific varieties of Eat Smart Salad Shake Ups after the Canadian Food Inspection Agency detected Listeria monocytogenes.
Product
Eat Smart Salad Shake Ups - Asian Sesame/Sesame Asiatique; 5.5 oz. (156 g); UPC 7 09351-30241 1, 7 09351 30244 2 Product of USA Distributed by Apio Inc., Guadalupe, Ca 93434
Category
Food
Distribution
14 states
SevereFDA (Food)·F-0822-2019·2019-01-02
Apio Recalls Eat Smart Salad Shake Ups Due to Listeria Risk
Apio, Inc. is recalling Eat Smart Salad Shake Ups after the Canadian Food Inspection Agency detected Listeria monocytogenes in the product.
Product
Eat Smart Salad Shake Ups - Tropical Lime/Lime Tropicale 5.5 oz. (156 g); US UPC 7 09351-30179 7; 7 09351 30197 1 Product of USA Distributed by Apio Inc., Guadalupe, Ca 93434
Category
Food
Distribution
14 states
SevereNHTSA·19V023000·2019-01-02
Ford Recalls 2019 EcoSport Vehicles Due to Improperly Welded Front Seat Frames
Ford is recalling 2019 EcoSport vehicles because improperly welded front seat frames may cause the seat back to be loose, increasing injury risk in a crash.
Product
FORD — FORD ECOSPORT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V022000·2019-01-02
Pierce Aerial Vehicles Recalled for Unexpected Ladder Rotation Defect
Pierce Manufacturing is recalling 2004-2018 aerial vehicles because the aerial device may unexpectedly rotate right during extension, increasing injury risk.
Product
PIERCE — PIERCE ENFORCER, DASH, QUANTUM, VELOCITY
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0683-2019·2019-01-02
Medtronic MiniMed Insulin Pumps Recalled for Missing Audio Alerts
Medtronic is recalling specific MiniMed insulin pump models because software version 4.10 may fail to play expected audio sounds during alerts, alarms, or sirens.
Product
Medtronic MiniMed 630G 6025805-003_C, Rx Only Medtronic MiniMed 670G 6025805-005_B, Rx Only Medtronic MiniMed 640G (International)
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0674-2019·2019-01-02
Tosoh Bioscience Recalls ST AIA-PACK Testosterone Diagnostic Test Kits
Tosoh Bioscience is voluntarily recalling ST AIA-PACK Testosterone kits due to a Class II defect. The recall covers 26,745 units distributed nationwide.
Product
ST AIA-PACK Testosterone (TES) is designed for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of testosterone in human serum on specific Tosoh AIA System analyzers. Measurement of testosterone is used to aid in the diagnosis and management of conditions involving…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0682-2019·2019-01-02
Radiometer ABL800 Analyzer Recalled for Potential Patient Data Mismatch
Radiometer America Inc is recalling 2,131 ABL800 analyzers because software may cause a mismatch between patient demographics and test results.
Product
ABL800 analyzer, model numbers 393-800 and 393-801.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0672-2019·2019-01-02
Tosoh Bioscience Recalls AIA-PACK Folate In Vitro Diagnostic Reagents
Tosoh Bioscience Inc is voluntarily recalling AIA-PACK Folate reagents used for in vitro diagnostic testing due to a Class II safety concern.
Product
AIA-PACK Folate (FOL) is designed for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of folate in human serum on Tosoh AIA System analyzers.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0673-2019·2019-01-02
Tosoh Bioscience Recalls ST AIA-PACK FT3 In Vitro Diagnostic Reagents
Tosoh Bioscience Inc is voluntarily recalling ST AIA-PACK FT3 reagents used for in vitro diagnostic testing of Free Triiodothyronine. The recall covers 24,083 units distributed nationwide.
Product
ST AIA-PACK FT3 (FT3: Free Triiodothyronine) is designed for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of Free Triiodothyronine (FT3) in human serum or heparinized plasma on specific Tosoh AIA System analyzers.
Category
Medical Device
Distribution
Distributed nationwide