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.

38076–38100 of 78725

ModerateFDA (Devices)·Z-0707-2019·2019-01-16
Siemens Biograph Horizon PET/CT System Recalled for Design Defects
Siemens Medical Solutions USA is recalling 171 Biograph Horizon PET/CT systems worldwide due to improper design or specifications.
Product
Siemens Biograph Horizon PET/CT System, Product Usage: The Siemens Biograph systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0375-2019·2019-01-16
Lupin Recalls Cefdinir Oral Suspension Due to CGMP Deviations
Lupin Pharmaceuticals is recalling Cefdinir for Oral Suspension because product complaints indicated the reconstituted suspension was observed to be thick.
Product
CEFDINIR — CEFDINIR (CEFDINIR)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·19V033000·2019-01-15
Bentley Recalls Mulsanne Vehicles Due to Rear Seat Belt Anchor Defect
Bentley is recalling 2012-2018 Mulsanne vehicles because the rear seat belt anchor may detach in a crash, increasing injury risk.
Product
BENTLEY — BENTLEY MULSANNE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V018000·2019-01-15
Chrysler Recalls Vehicles Due to Exploding Passenger Air Bag Inflator Risk
Chrysler is recalling specific 2010-2016 Dodge, Chrysler, and Jeep vehicles because the passenger air bag inflator may explode during deployment, potentially causing serious injury or death.
Product
DODGE — DODGE, CHRYSLER, JEEP CHALLENGER, CHARGER, 300, WRANGLER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V015000·2019-01-14
BMW Recalls 2000-2004 Models for Air Bag Inflator Explosion Risk
BMW is recalling specific 2000-2004 5 Series and X5 vehicles because the air bag inflator in optional sports steering wheels may explode, posing a serious injury risk.
Product
BMW — BMW 540I, 525I, X5 SAV, 530I
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V016000·2019-01-14
BMW Recalls 2015 X1 Vehicles for Driver Air Bag Inflator Defect
BMW is recalling 2015 X1 vehicles because the driver's air bag inflator may explode due to humidity, posing a risk of serious injury or death.
Product
BMW — BMW X1 SAV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V017000·2019-01-14
BMW Recalls X5 and X6 Models Due to Air Bag Inflator Defect
BMW is recalling 2007-2014 X5 and X6 models because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Product
BMW — BMW X5, X6
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V032000·2019-01-14
Volvo Recalls 2018-2019 VNL Trucks for Clutch Assembly Defect
Volvo is recalling 2018-2019 VNL trucks with automated manual transmissions because a clutch component may fail, causing unintended vehicle movement.
Product
VOLVO — VOLVO VNL
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V031000·2019-01-14
Ford Recalls 2019 Lincoln Nautilus for Lane Center Assist Defect
Ford is recalling 2019 Lincoln Nautilus vehicles because the Lane Center Assist system may fail to detect if the driver's hands are off the steering wheel for a prolonged period.
Product
LINCOLN — LINCOLN NAUTILUS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V014000·2019-01-11
Volkswagen and Audi Recall Vehicles Due to Airbag Inflator Defect
Volkswagen is recalling specific 2015-2017 models because the driver's airbag inflator may explode during deployment, potentially causing serious injury.
Product
AUDI — AUDI, VOLKSWAGEN TT ROADSTER, CC, R8 SPYDER, EOS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V029000·2019-01-11
Double K Recalls 2017-2018 Hometown Trolley Buses for Brake Bolt Issue
Double K is recalling 2017-2018 Hometown Trolley buses because loose brake caliper bolts may reduce braking effectiveness and increase crash risk.
Product
HOMETOWN TROLLEY — HOMETOWN TROLLEY STREETCAR, MAINSTREET, VILLAGER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V030000·2019-01-11
Double K Recalls 2017-2019 Hometown Trolley Buses for Brake Bolt Issue
Double K is recalling 2017-2019 Hometown Trolley buses because brake caliper bolts may loosen, reducing brake effectiveness and increasing crash risk.
Product
HOMETOWN TROLLEY — HOMETOWN TROLLEY STREETCAR, VILLAGER, MAINSTREET
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V028000·2019-01-11
HME 1871 Recall: Whelen Brake Lights May Illuminate Incorrectly
HME is recalling 2017-2018 1871 vehicles with Whelen accessory brake lights that may falsely illuminate, increasing crash risk.
Product
HME — HME 1871
Category
Vehicle
Distribution
Distributed nationwide
CriticalNHTSA·19V008000·2019-01-09
Subaru Recalls Vehicles Due to Passenger Air Bag Inflator Explosion Risk
Subaru is recalling specific 2010-2014 models because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Product
SUBARU — SUBARU OUTBACK, FORESTER, LEGACY, IMPREZA
Category
Vehicle
Distribution
Distributed nationwide
CriticalNHTSA·19V010000·2019-01-09
Mercedes-Benz Recalls Vehicles Due to Passenger Air Bag Inflator Defect
Mercedes-Benz is recalling specific 2010-2017 models because passenger air bag inflators may explode due to humidity, posing a risk of serious injury or death.
Product
MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ C300, E350, GLK350, C350
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0552-2019·2019-01-09
Medtronic StealthStation Cranial Software Recall for Biopsy Depth Gauge Error
Medtronic is recalling StealthStation Cranial and Synergy Cranial software due to an incorrect display of the Biopsy Depth Gauge that resulted in the biopsy of healthy tissue.
Product
StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation Cranial Optical Pocket Guide - Instructions for cranial procedures using optical localization StealthStation Cranial version 3.0, 3.1 CE 0344 Rx Only 2018-02 9735489 Revision 3 Medtronic Navigation, Inc.…
Category
Medical Device
Distribution
51 states
SevereNHTSA·19V005000·2019-01-09
Toyota Recalls Vehicles for Front Passenger Air Bag Inflator Defect
Toyota is recalling approximately 1.3 million vehicles because front passenger air bag inflators may explode due to humidity, potentially causing serious injury or death.
Product
LEXUS — LEXUS, TOYOTA, SCION IS F, COROLLA, COROLLA MATRIX, 4RUNNER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V009000·2019-01-09
Subaru Recalls Vehicles Due to Air Bag Inflator Explosion Risk
Subaru is recalling specific 2010-2014 models because passenger air bag inflators may explode during deployment, potentially causing serious injury or death.
Product
SUBARU — SUBARU OUTBACK, FORESTER, LEGACY, IMPREZA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V007000·2019-01-09
Subaru Recalls Vehicles Due to Front Passenger Air Bag Inflator Defect
Subaru is recalling specific 2010-2014 models because front passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Product
SUBARU — SUBARU OUTBACK, FORESTER, LEGACY, IMPREZA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V006000·2019-01-09
Ferrari Recalls Multiple Models Due to Passenger Air Bag Inflator Defect
Ferrari is recalling various models from 2014 to 2018 because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Product
FERRARI — FERRARI CALIFORNIA T, FF, F12 BERLINETTA, 488 GTB
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0688-2019·2019-01-09
Ortho-Clinical Diagnostics Recalls VITROS HBeAg Reagent Due to Biased Results
Ortho-Clinical Diagnostics is extending a 2018 recall of VITROS HBeAg Reagent because biotin interference may cause inaccurate test results.
Product
VITROS HBeAg Reagent, Cat. No 6801819 Product Usage: For the in vitro qualitative detection of hepatitis B e antigen (HBeAg) in human adult and pediatric (2 to 21 years old) serum from individuals who have symptoms of hepatitis or who may be at risk for hepatitis B virus…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0689-2019·2019-01-09
Ortho-Clinical Diagnostics Recalls VITROS NT-proBNP Reagent for Biased Results
Ortho-Clinical Diagnostics is extending a 2018 recall of VITROS NT-proBNP Reagent because it may produce biased results at low biotin concentrations.
Product
VITROS NT-proBNP Reagent, Cat No. 6802156 Product Usage: For in vitro diagnostic use only. For the quantitative measurement of N-terminal pro Brain Natriuretic Peptide (NT-proBNP) in human serum and plasma (EDTA or heparin) using the VITROS ECi/ECiQ Immunodiagnostic Systems…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0687-2019·2019-01-09
Ortho-Clinical Diagnostics Recalls VITROS Anti-HBe Reagent Packs
Ortho-Clinical Diagnostics is recalling VITROS Anti-HBe Reagent Packs because biased results may occur at lower biotin concentrations than indicated in the instructions.
Product
VITROS Anti-HBe Reagent Pack, Cat No. 6801816 Product Usage: For the in vitro qualitative detection of antibodies to hepatitis B e antigen (anti-HBe) in human adult and pediatric (2 to 21 years old) serum from individuals who have symptoms of chronic hepatitis and those who…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0346-2019·2019-01-09
Lupin Recalls Subpotent Nitrofurantoin Oral Suspension Lots
Lupin Pharmaceuticals is recalling specific lots of Nitrofurantoin Oral Suspension because the drug was found to contain less active ingredient than required.
Product
NITROFURANTOIN — NITROFURANTOIN (NITROFURANTOIN)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0690-2019·2019-01-09
Ultradent Recalls Enamelast Fluoride Varnish Due to Off-Flavor Complaints
Ultradent Products, Inc. is recalling specific lots of Enamelast 5% Sodium Fluoride Varnish because the product may have an unpleasant or off flavor.
Product
Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Dose 200pk Cool Mint: Enamelast 5% Sodium Fluoride Unit Dose 200pk Kit - Cool Mint REF/UP 4352 Rx CONTENTS: 200 x 0.4 ml Unit Dose Label Enamelast Unit Dose 50pk Cool Mint: Enamelast 5% Sodium…
Category
Medical Device
Distribution
Distributed nationwide