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.

38651–38675 of 78725

ModerateFDA (Devices)·Z-0399-2019·2018-11-14
Zimmer Biomet Recalls StageOne Hip Cement Spacer Molds
Zimmer Biomet is recalling 72 units of StageOne Hip cement spacer molds due to a potential for comingling of 43MM and 51MM sizes.
Product
StageOne Hip, Models 431207 & 431209Usage: Product Usage: The single-use cement spacer molds are sterile disposables made of medical grade silicone with a 316L stainless steel reinforcement stem. They are designed to be filled with polymethylmethacrylate/gentamicin bone…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0222-2019·2018-11-14
Baxter Recalls Metoprolol Tartrate Injection Due to pH Specification Failures
Baxter Healthcare is recalling 402,165 vials of Metoprolol Tartrate Injection because the solution's pH shifted upward during shelf life.
Product
METOPROLOL — METOPROLOL (METOPROLOL TARTRATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0218-2019·2018-11-14
Janssen Recalls Ortho-Novum 7/7/7 Tablets Due to Incorrect Dispenser Instructions
Janssen Pharmaceuticals is recalling Ortho-Novum 7/7/7 tablets because the packaging included instructions for the wrong type of pill dispenser.
Product
Ortho-Novum 7/7/7 (norethindrone/ethinyl/estradiol) Tablets, 0.5 mg/0.035 mg, 0.75 mg/0.035 mg, 1 mg/0.035, 28-Day Regimen per pouch, packaged in a) 6 Veridate Tablet Dispensers and 6 Refill pouches (NDC 504-58-178-28) per carton (NDC 50458-178-06); and b) 12 Veridate Tablet…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0256-2019·2018-11-14
Healthful Naturals Leg Cramp Support Oral Spray Recalled for CGMP Deviations
Silver Star Brands is recalling Healthful Naturals Leg Cramp Support Oral Spray due to manufacturing deviations that could result in possible microbial contamination.
Product
Healthful Naturals Leg Cramp Support Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906 NDC 68703-206-02
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0392-2019·2018-11-14
Ortho-Clinical Diagnostics Recalls VITROS Vitamin B12 Reagent Packs
Ortho-Clinical Diagnostics is recalling VITROS Vitamin B12 Reagent Packs due to a potential for increased calibration failures.
Product
VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2, Catalog Number 1453489 For in vitro diagnostic use only For the quantitative measurement of vitamin B12 in human serum and plasma (EDTA or heparin) using the VITROS ECi/ECiQ Immunodiagnostic Systems, the VITROS…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0383-2019·2018-11-14
Qiagen EZ1 Advanced XL Recalled for Potential Heater Malfunction
Qiagen is recalling 298 EZ1 Advanced XL instruments due to a power board defect that may cause heater malfunctions and compromise nucleic acid extractions.
Product
EZ1 Advanced XL, Model Number: 9001492, GTIN: 04053228010760 Product Usage: The EZ1 Advanced XL is designed to perform automated isolation and purification of nucleic acids. It is intended to be used only in combination with QIAGEN kits indicated for use with the EZ1…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0385-2019·2018-11-14
CareFusion Recalls Alaris Infusion Pump Administration Sets Due to Priming Issues
CareFusion 303, Inc. is recalling Alaris Infusion Pump administration sets because users reported being unable to prime the devices.
Product
Alaris Infusion Pump administration sets labeled as: -Infusion Set Alaris Pump Module/Medley Pump Module/Gemini Infusion Pump, REF 10011301, CareFusion, WARNING: TO PREVENT FREE-FLOW, CLOSE SET CLAMP WHEN SAFETY CLAMP FITMENT ON PUMP SEGMENT IS OPEN, Fluid path is STERILE and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0217-2019·2018-11-14
Janssen Recalls Ortho-Novum 1/35 Due to Incorrect Dispenser Instructions
Janssen Pharmaceuticals is recalling Ortho-Novum 1/35 tablets because the packaging included instructions for the wrong type of pill dispenser.
Product
Ortho-Novum 1/35 (norethindrone/ethinyl estradiol) Tablets, 1 mg/0.035 mg, 28-Day Regimen per pouch (NDC 50458-176-28), 6 Veridate Tablet Dispensers and 6 refills per carton (NDC 50458-176-06), Rx only, Manufactured by: Janssen Ortho, LLC, Manati, Puerto Rico 00674; Manufactured…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0223-2019·2018-11-14
Tailor Made Compounding Recalls Tesamorelin Vials Due to Incorrect Expiration Dates
Tailor Made Compounding is recalling 10,280 vials of Tesamorelin because the labels indicate a 1-year expiration date instead of the correct 6-month date.
Product
Tesamorelin, 1mg/vial, 6mL vial, Lyophilized Powder for Reconstitution and Subcutaneous Injection, Rx Only, Tailor Made Compounding, Nicholasville, KY 40356
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0404-2019·2018-11-14
Medtronic Navigation 0-arm 02 Imaging System Software and Hardware Recall
Medtronic Navigation is recalling 641 O-arm 02 Imaging Systems to correct software version 4.1.0, update manuals and labels, and replace blown fuses in the AC power input circuit.
Product
Medtronic Navigation 0-arm 02 Imaging System interventional fluoroscopic x-ray system: OARM BI70002000 SYS IMAGING 02 Model: BI70002000 OARM BI70002000R SYS IMAGING 02 REFURB Model: BI70002000R
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0377-2019·2018-11-14
AROA Endoform Dermal Template Recalled for Potential Pouch Seal Failure
AROA Biosurgery is recalling Endoform Dermal Template 2x2 units due to a potential for pouch seal failure.
Product
Endoform Dermal Template 2x2, SKU 529311 Product Usage: Endoform Dermal Template is a sterile, single use ovine forestomach derived extracellular matrix intended to cover, protect and provide a moist wound environment.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0247-2019·2018-11-14
Medline Recalls SparkleFresh Toothpaste Due to Microbial Contamination
Medline Industries is recalling SparkleFresh fluoride toothpaste nationwide due to microbial contamination of the non-sterile product.
Product
SPARKLEFRESH — SPARKLEFRESH (SODIUM MONOFLUOROPHOSPHATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0405-2019·2018-11-14
Integrity Implants Recalls FlareHawk Interbody Fusion System Instructions for Use
Integrity Implants is correcting Instructions for Use for the FlareHawk Interbody Fusion System due to discrepancies in cleaning parameters.
Product
FlareHawk Interbody Fusion System (previously XCage Interbody Fusion System) Instructions for Use (IFU's) only. Product Usage: Indicated for spinal intervertebral body fusion with autogenous bone graft in skeletally mature individuals with degenerative disc disease.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0389-2019·2018-11-14
Medtest AutoHDL/LDL Cholesterol Calibrator Recalled for Missing Vial Labels
Medtest Holdings is recalling 22 vials of AutoHDL/LDL Cholesterol Calibrator shipped without labels in five states.
Product
Pointe Scientific AutoHDL/LDL Cholesterol Calibrator, Catalog Number H7545-CAL - Product Usage: For the calibration of Pointe Scientific s autoHDL and autoLDL Cholesterol Reagent Set in serum or plasma. For in vitro diagnostic use only.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·19715·2018-11-13
YTL International Recalls County Line Log Splitters Due to Injury Hazard
YTL International is recalling about 1,460 County Line log splitters because welding on the tongue box assembly can crack, causing the tank to disconnect and posing an injury hazard.
Product
County Line log splitters
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·18V800000·2018-11-13
Volvo Recalls 2017-2019 Models Due to Telematics Software Error
Volvo is recalling 2017-2019 models because a software error may prevent GPS location data from reaching emergency personnel during a crash.
Product
VOLVO — VOLVO XC90, V60, S90, XC60
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V796000·2018-11-12
Coach and Equipment Recalls 2015-2018 Phoenix and Metro Lite Buses
Coach and Equipment is recalling 864 transit buses because foldaway seats may not lock properly, increasing injury risk in crashes.
Product
COACH AND EQUIPMENT — COACH AND EQUIPMENT PHOENIX, METRO LITE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V798000·2018-11-12
Champion and Goshen Transit Buses Recalled for Seat Lock Defect
Champion Bus is recalling 2017-2018 transit buses because foldaway seats may not stay locked during a crash or sudden stop, increasing injury risk.
Product
CHAMPION — CHAMPION, GOSHEN LF TRANSPORT, CHALLENGER, G-FORCE, IMPULSE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V799000·2018-11-12
Starcraft Transit Bus Recall for Foldaway Seat Locking Defect
Forest River is recalling specific Starcraft transit buses because foldaway seat cushions may not stay locked in a crash, increasing injury risk.
Product
STARCRAFT BUS — STARCRAFT BUS, STARCRAFT SENATOR II, ALLSTAR, STARLITE, STARQUEST
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18E104000·2018-11-12
BatteryJack Recalls Certain Adult Motorcycle Helmets for Impact Protection Defects
BatteryJack is recalling specific adult motorcycle helmets that may not adequately protect wearers during a crash and may have improper labeling.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·18V789000·2018-11-09
Gillig Recalls 2013-2018 Low Floor Buses Due to Parking Brake Defect
Gillig is recalling 2013-2018 Low Floor transit buses because loose spring cage bolts may reduce parking brake effectiveness, increasing crash risk.
Product
GILLIG — GILLIG LOW FLOOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V792000·2018-11-09
Altec Recalls 2017-2018 Aerial Devices Due to Wiring Fire Risk
Altec is recalling 186 aerial devices from 2017-2018 because under-hood wiring may be damaged by sharp edges, increasing the risk of a fire.
Product
ALTEC — ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V794000·2018-11-09
Terex Recalls 2017-2018 Digger Derrick Vehicles Due to Weld Defect
Terex is recalling 2017-2018 Digger Derrick vehicles because insufficient welds on the guide bar may cause the guide arm to fall, posing an injury risk to nearby personnel.
Product
TEREX — TEREX DIGGER DERRICK
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V788000·2018-11-09
Eldorado National Recalls 2014-2018 Vans Due to Seat Lock Defect
Eldorado National is recalling 2014-2018 Aerolite, Aerotech, Impulse, and World Trans vans because foldaway seats may not stay locked during a crash, increasing injury risk.
Product
GOSHEN — GOSHEN, ELDORADO IMPULSE, AEROLITE, AEROTECH, WORLD TRANS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V791000·2018-11-09
Altec Cranes and Digger Derricks Recalled for Wiring Fire Risk
Altec is recalling 2008-2018 cranes and digger derricks because undersized wiring may overheat and cause a fire. Owners should contact Altec for a free repair.
Product
ALTEC — ALTEC CRANE, DIGGER DERRICK
Category
Vehicle
Distribution
Distributed nationwide