State

Utah product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52576–52600 of 78749

ModerateFDA (Drugs)·D-0840-2016·2016-05-18
Mylan Recalls Paliperidone Extended-Release Tablets Due to Dissolution Failures
Mylan Pharmaceuticals is recalling 2,928 bottles of Paliperidone Extended-Release Tablets, 1.5 mg, because they failed dissolution specifications at a three-month stability time point.
Product
Paliperidone Extended-release Tablets, 1.5 mg, 30 count bottles, Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV --- NDC 0378-3978-93
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1657-2016·2016-05-18
Siemens ADVIA Chemistry Triglycerides Reagent Recalled for Interference
Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Triglycerides reagents because N-Acetylcysteine and Metamizole can cause falsely depressed test results.
Product
ADVIA CHEMISTRY TRIGLYCERIDES_2 (TRIG_2) REAGENT & ADVIA CHEMISTRY TRIGLYCERIDES_2 Concentrated (TRIG_c) REAGENT
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1622-2016·2016-05-18
Siemens Recalls Dimension Vista BUN Reagent Cartridges for Inaccurate Results
Siemens Healthcare Diagnostics is recalling specific lots of Dimension Vista BUN Flex reagent cartridges because they may produce inaccurate patient or quality control results.
Product
Dimension Vista Blood Urea Nitrogen (BUN) Flex reagent cartridge The BUN method is an in vitro diagnostic test for the quantitative measurement of urea nitrogen (an end product of nitrogen metabolism) in human serum, plasma, and urine on the Dimension Vista System.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1628-2016·2016-05-18
Baxter Recalls GEM FlowCoupler Devices Due to Packaging Defect
Baxter Healthcare is recalling 630 units of GEM FlowCoupler devices because the instructions for use booklet may puncture the outer Tyvek lid.
Product
GEM(TM), FLOWCOUPLER(R), 2.5 mm, STERILE EO, Rx only, 1 FLOWCOUPLER, REF GEM2753-FC. Product Usage: The FlowCOUPLER Device is a single use, implantable device that is intended to be used in the end-to-end anastomosis of veins and arteries normally encountered in…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1627-2016·2016-05-18
Baxter GEM Flowcoupler Recall Due to Packaging Puncture Risk
Baxter Healthcare is recalling 315 units of GEM Flowcoupler devices because the instructions for use booklet may puncture the outer Tyvek lid.
Product
GEM(TM), FLOWCOUPLER(R), 2.0 mm, STERILE EO, Rx only, 1 FLOWCOUPLER, REF GEM2752-FC Product Usage: The FlowCOUPLER Device is a single use, implantable device that is intended to be used in the end-to-end anastomosis of veins and arteries normally encountered in microsurgical…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0852-2016·2016-05-18
Baxter Recalls Brevibloc Injection Due to Yellow Discoloration
Baxter Healthcare is recalling Brevibloc (esmolol hydrochloride) injection because the solution shows atypical yellow discoloration. The recall covers 11,630 units distributed nationwide.
Product
BREVIBLOC — BREVIBLOC (ESMOLOL HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1659-2016·2016-05-18
Siemens Direct HDL Cholesterol Assay Recalled for Interference
Siemens is recalling Direct HDL Cholesterol assays because N-Acetylcysteine and Metamizole can cause falsely depressed results.
Product
Dimension Assays: Direct HDL Cholesterol (AHDL)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1631-2016·2016-05-18
Baxter GEM FlowCoupler Recalled Due to Packaging Lid Puncture Risk
Baxter Healthcare is recalling 118 units of GEM FlowCoupler devices because the instructions for use booklet may puncture the outer Tyvek lid.
Product
GEM(TM), FLOWCOUPLER(R), 4.0 mm, STERILE EO, Rx only, 1 FLOWCOUPLER, REF GEM2756-FC Product Usage: The FlowCOUPLER Device is a single use, implantable device that is intended to be used in the end-to-end anastomosis of veins and arteries normally encountered in microsurgical…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1630-2016·2016-05-18
Baxter Recalls GEM FlowCOUPLER Due to Packaging Lid Puncture Risk
Baxter Healthcare is recalling 288 units of GEM FlowCOUPLER devices because the instructions for use booklet may puncture the outer Tyvek lid.
Product
GEM(TM), FLOWCOUPLER(R), 3.5 mm, STERILE EO, Rx only, 1 FLOWCOUPLER, REF GEM2755-FC Product Usage: The FlowCOUPLER Device is a single use, implantable device that is intended to be used in the end-to-end anastomosis of veins and arteries normally encountered in microsurgical…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1652-2016·2016-05-18
Siemens LDL Cholesterol Assay Recalled for Interference
Siemens is recalling Advia Chemistry Assay: LDL Cholesterol, Direct because N-Acetylcysteine and Metamizole can cause falsely depressed results.
Product
Advia Chemistry Assay: LDL Cholesterol, Direct
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1658-2016·2016-05-18
Siemens Uric Acid Assay Recalled Due to Interference
Siemens Healthcare Diagnostics is recalling Uric Acid assays because N-Acetylcysteine and Metamizole can cause falsely depressed results.
Product
Advia Chemistry Assay: Uric Acid and Uric Acid, concentrated
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0841-2016·2016-05-18
Dr. Reddy's Recalls Ondansetron Tablets Due to Failed Impurity Specifications
Dr. Reddy's Laboratories is recalling 50,280 bottles of Ondansetron Tablets USP, 4 mg, due to failed impurities and degradation specifications.
Product
Ondansetron Tablets USP, 4 mg, 30 count bottles, Rx only, Manufactured by: Dr. Reddy's Laboratories, Bachupally, India --- NDC 56111-153-30
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1629-2016·2016-05-18
Baxter Recalls GEM FlowCoupler Devices Due to Packaging Defect
Baxter Healthcare is recalling 707 units of GEM FlowCoupler devices because the instructions for use booklet may puncture the outer Tyvek lid.
Product
GEM(TM), FLOWCOUPLER(R), 3.0 mm, STERILE EO, Rx only, 1 FLOWCOUPLER, REF GEM2754-FC Product Usage: The FlowCOUPLER Device is a single use, implantable device that is intended to be used in the end-to-end anastomosis of veins and arteries normally encountered in microsurgical…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1615-2016·2016-05-18
Siemens ADVIA Centaur CP Immunoassay System Recalled for Documentation Errors
Siemens Healthcare Diagnostics is recalling the ADVIA Centaur CP Immunoassay System because inaccuracies in the Operator's Guide may cause sample processing issues when using EZee-Nest Insert Cups.
Product
ADVIA Centaur CP Immunoassay System, Siemens Material Number (SMN) 10309710, IVD. --- CLASSIFICATION NAME: Immunoassay Analyzers. This system is intended for professional use in a laboratory environment only. Tests performed using this system are intended for in vitro…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·16E045000·2016-05-17
Bendix SR-5 Trailer Spring Brake Valves Recalled for Parking Brake Delay
Bendix is recalling SR-5 Trailer Spring Brake Valves manufactured between January 2014 and March 2016 because improper machining may delay spring brake application, increasing the risk of trailers rolling away.
Product
PARKING BRAKE recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V311000·2016-05-17
BMW Recalls 2011 X5 and X6 Models for Driveshaft Defect
BMW is recalling 21,493 2011 X5 and X6 vehicles because a front driveshaft joint may fail, increasing crash risk.
Product
BMW — BMW X6 ACTIVEHYBRID SAC, X5 DIESEL SAV, X5, X6
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V313000·2016-05-17
Spartan K3 and MM Motorhome Chassis Recalled for Exhaust Fire Risk
Spartan is recalling 2007-2015 K3 and MM motorhome chassis because a torn flexible exhaust tube may allow hot gas to contact other components, increasing fire risk.
Product
SPARTAN — SPARTAN K3, MM
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V310000·2016-05-17
Collins Recalls 2016 School Buses Due to Seat Separation Risk
Collins Bus Corporation is recalling 2016 DH416 and DE516 school buses because seats may separate from the base frame due to bolt failure, increasing injury risk in a crash.
Product
COLLINS — COLLINS DH416, DE516
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V309000·2016-05-17
Eldorado Transit Bus Recall for Seat Separation Risk
Eldorado is recalling 2016 Advantage and Aerotech transit buses because seats may separate from the base frame due to bolt failure, increasing injury risk in a crash.
Product
ELDORADO — ELDORADO AEROTECH, ADVANTAGE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V312000·2016-05-17
Kia Recalls 2013 Fortes Due to Front Seatbelt Retainer Defect
Kia is recalling 2013 Fortes because front seatbelt retractor screws may be loose. This could cause the retractor plate to break in a crash, striking occupants.
Product
KIA — KIA FORTE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V308000·2016-05-17
Mercedes-Benz Recalls 2016 AMG GT S for Driveshaft Bond Failure
Mercedes-Benz is recalling 136 model year 2016 AMG GT S vehicles because the carbon-fiber driveshaft bond may fail, causing loss of torque and increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ AMG GT S
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·16162·2016-05-17
Pacific Cycle Recalls Infant Bicycle Helmets Due to Choking and Magnet Hazards
Pacific Cycle is recalling about 129,000 infant bicycle helmets sold at Target because loose magnetic buckle parts pose choking and ingestion risks to young children.
Product
Infant bicycle helmets with magnetic no-pinch buckle chin straps
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·16159·2016-05-17
Target Recalls Acrylic Hanukkah Menorahs Due to Fire Hazard
Target is recalling clear acrylic Hanukkah menorahs because they can melt when candles are burning, posing a fire hazard. No injuries or property damage have been reported.
Product
Menorahs
Category
Consumer Product
Distribution
Distributed nationwide
CriticalNHTSA·16E043000·2016-05-16
Takata Frontal Passenger Air Bag Inflator Recall for Humidity-Related Rupture Risk
Takata is recalling specific frontal passenger air bag inflators that may rupture due to humidity exposure, posing a risk of serious injury or death from metal fragments.
Product
AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
CriticalNHTSA·16E044000·2016-05-16
Takata Frontal Passenger Air Bag Inflator Recall for Specific States
Takata is recalling specific frontal passenger air bag inflators used in vehicles registered in 22 states due to a risk of rupture.
Product
AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
Category
Vehicle
Distribution
Distributed nationwide