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.

50901–50925 of 78749

ModerateFDA (Devices)·Z-2344-2016·2016-08-17
Siemens Artis Angiography Systems Recalled for Image Reproduction Failure
Siemens Medical Solutions is recalling 51 Artis zee and Artis Q angiography systems due to a software error that may cause image loss after startup.
Product
Artis zee/ zeego, Artis Q/ Q.zen, stand alone system, software controlled Model numbers: 10094135, 10094137, 10094139, 10094141, 10280959, 10848281, 10848282, 10848283, 10848353, 10848255 Artis zee / zeego and Q/ Q.zen is a family of dedicated angiography systems developed for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2384-2016·2016-08-17
Philips Ingenuity CT Software Recall for Performance Issues
Philips is recalling Ingenuity Core128 CT scanners due to software issues in versions 4.1.3, 4.1.4, and 4.1.5 that could affect equipment performance.
Product
Ingenuity Core128 Model No. 728323; To produce cross-sectional images of the body.
Category
Medical Device
Distribution
45 states
ModerateFDA (Devices)·Z-2372-2016·2016-08-17
Philips Ingenuity Core 128 CT Systems Recalled for Software Defect
Philips is recalling five Ingenuity Core 128 CT systems due to a software defect causing intermittently slow response of the Host.
Product
Ingenuity Core 128 Computed Tomography X-ray systems is intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
46 states
ModerateFDA (Devices)·Z-2394-2016·2016-08-17
Siemens AXIOM Artis X-Ray Systems Recalled for Cooling System Contamination
Siemens is recalling AXIOM Artis angiography systems because biomass contaminants in the cooling system may damage the pump.
Product
ARTIS ZEE AND ZEEGO, system, x-ray, angiographic AXIOM Artis, Artis zee / zeego and Artis Q/ Q.zen are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2364-2016·2016-08-17
Invacare Pediatric Flowmeter Recalled for Upside-Down Rear Scale Printing
Invacare is recalling 395 Precise Rx Pediatric Flowmeters because the rear gradation scale was printed upside down, which may cause confusion during oxygen flow monitoring.
Product
lnvacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16. Packed one per carton. The lnvacare Precise Rx Pediatric Flowmeter adapts to lnvacare Concentrators for low-flow usage.The gauge has a scale printed on the front side and the back side. The front scale is the…
Category
Medical Device
Distribution
30 states
ModerateFDA (Food)·F-1875-2016·2016-08-17
Healthwise Protein Chips Recalled Due to Foreign Plastic Matter
Nutritional Resources Inc. is recalling Healthwise Protein Chips because foreign plastic was observed in the product.
Product
Healthwise, Protein Chips, Barbecue Crunch, Net Weight 1.2 ounces (34 grams), Distributed by Nutritional Resources, Inc., Grovetown, GA 30813.
Category
Food
Distribution
39 states
ModerateFDA (Devices)·Z-2405-2016·2016-08-17
Topcon Recalls PASCAL Synthesis Ophthalmic Laser Systems Due to Titration Anomaly
Topcon Medical Laser Systems is recalling 205 PASCAL Synthesis ophthalmic laser systems worldwide due to a software anomaly affecting the titration process when specific functions are used.
Product
Opthalmic: PASCAL Synthesis is an ophthalmic scanning laser system. The system can perform single shot photocoagulation as is performed conventionally.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2366-2016·2016-08-17
Philips Brilliance 64 CT Systems Recalled for Software Defect
Philips Medical Systems is recalling 318 Brilliance 64 Computed Tomography X-ray systems due to a software defect causing intermittently slow response of the Host.
Product
Brilliance 64 Computed Tomography X-ray systems is intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
46 states
ModerateFDA (Devices)·Z-2371-2016·2016-08-17
Philips Ingenuity Core CT Systems Recalled for Software Defect
Philips Medical Systems is recalling 29 Ingenuity Core CT systems due to a software defect causing intermittently slow response of the Host.
Product
Ingenuity Core Computed Tomography X-ray systems is intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
46 states
ModerateFDA (Devices)·Z-2395-2016·2016-08-17
Siemens Medical Solutions Recalls Artis Q and Q.Zen Angiography Systems
Siemens Medical Solutions is recalling Artis Q and Q.Zen angiography systems because biomass in the cooling system may damage the pump.
Product
ARTIS Q AND Q.ZEN- MODULAR ANGIOGRAPHIC SYSTEM, interventional fluoroscopic x-ray system22 AXIOM Artis, Artis zee / zeego and Artis Q/ Q.zen are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2375-2016·2016-08-17
Nobel Biocare Recalls Guided Surgery Kit Instructions for Incorrect Drill Protocol
Nobel Biocare is recalling 231 Guided Surgery Kits because the Instructions for Use contain an incorrect drill protocol. The kits are used for NobelParallel CC Implants.
Product
Instructions for Use (IFU) and Manual NobPrl CC Guided Surgery Kit Instructions for Use (IFU): "NobelGuide for NobelParallel Conical Connection", id # 2002 and Manual: Guided Surgery with NobelParallel Conical Connection", id # 79423. Article # 38072, Nobel Parallel CC Guided…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2365-2016·2016-08-17
Invacare Pediatric Flowmeter Recalled Due to Upside-Down Rear Scale
Invacare is recalling 395 Precise Rx Pediatric Flowmeters because the rear gradation scale was printed upside down, which may confuse users.
Product
Invacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16 AW. Packed one per carton. The lnvacare Precise Rx" Pediatric Flowmeter adapts to lnvacare Concentrators for low-flow usage.The gauge has a scale printed on the front side and the back side. The front scale is the…
Category
Medical Device
Distribution
30 states
ModerateFDA (Devices)·Z-2381-2016·2016-08-17
Philips Brilliance iCT Recalled for Software Performance Issues
Philips Medical Systems is recalling 335 Brilliance iCT units due to software issues in versions v4.1.3 and v4.1.5 that could affect equipment performance.
Product
Brilliance iCT, Model No. 728306; To produce cross-sectional images of the body.
Category
Medical Device
Distribution
45 states
ModerateFDA (Devices)·Z-2393-2016·2016-08-17
Siemens AXIOM Artis Angiography Systems Recalled for Cooling System Contamination
Siemens is recalling AXIOM Artis angiography systems because biomass contamination in the cooling system may damage the pump.
Product
AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM, system, x-ray, angiographic AXIOM Artis, Artis zee / zeego and Artis Q/ Q.zen are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2369-2016·2016-08-17
Philips Brilliance 16 CT Systems Recalled for Software Defect
Philips Medical Systems is recalling 203 Brilliance 16 CT systems due to a software defect causing intermittently slow response of the Host.
Product
Brilliance 16 Computed Tomography X-ray systems is intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
46 states
ModerateFDA (Devices)·Z-2370-2016·2016-08-17
Philips Brilliance CT 16 Power Systems Recalled for Software Defect
Philips Medical Systems is recalling 55 Brilliance CT 16 Power systems due to a software defect causing intermittently slow response of the Host.
Product
Brilliance CT 16 Power Computed Tomography X-ray systems is intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
46 states
LowFDA (Devices)·Z-2378-2016·2016-08-17
BD Tritest CD3/CD4/CD45 Reagent Recalled for Incorrect Labeling
Becton, Dickinson and Company is recalling 14,089 vials of BD Tritest CD3 FITC/CD4 PE/CD45 PerCP because the label incorrectly states the product contains gelatin.
Product
BD Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD); Catalog number 340383. Label states: Contains CD3 FITC/CD4 PE/CD45 per CP with Gelatin and 0.1% sodium azide. Hematology: BD Tritest CD3 fluorescein isothiocyanate (FITC)/CD4 phycoerythrin (PE)/CD45 peridinin chlorophyll…
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·16767·2016-08-16
Sauder Woodworking Recalls Storybook Four-Drawer Chests for Tip-Over Hazard
Sauder Woodworking is recalling about 8,000 Storybook four-drawer chests sold at Walmart.com due to a serious tip-over hazard that could injure children.
Product
Four-drawer chests
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·16V606000·2016-08-16
KME Predator Emergency Vehicles Recalled for Front Grille Separation Risk
Kovatch Mobile Equipment is recalling 27 KME Predator emergency vehicles from 2012-2013 because the front grille may loosen and separate from the cab, creating a road hazard.
Product
KME — KME PREDATOR AERIAL, PREDATOR PUMPER, PREDATOR RESCUE, PREDATOR PANTHER PUMPER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V603000·2016-08-16
Mercedes-Benz Recalls 2016 C300 and GLC300 for Electronic Stability Control Defect
Mercedes-Benz is recalling 2016 C300 and GLC300 vehicles because a damaged Electronic Stability Program control unit may activate stability control or disable the parking brake, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ C300, GLC300
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V599000·2016-08-15
Autocar Recalls 2016-2017 Xspotter Vehicles for Steering Column Defect
Autocar is recalling 294 model year 2016-2017 Xspotter vehicles because a steering column shaft weld may break, causing a loss of steering ability and increasing crash risk.
Product
AUTOCAR — AUTOCAR XSPOTTER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V601000·2016-08-15
Spartan Motors Recalls 2014-2016 Legend and Star Fire Trucks
Spartan Motors is recalling 2014-2016 Legend and Star fire trucks due to a transmission defect that may prevent power output switching, risking injury.
Product
SPARTAN ERV — SPARTAN ERV LEGEND, STAR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V600000·2016-08-15
Keystone Recalls 2011-2017 Bullet and Passport Trailers for Fire Risk
Keystone is recalling 2011-2017 Bullet and Passport recreational trailers because an improperly wired air conditioner thermostat may cause an electrical short and fire.
Product
KEYSTONE — KEYSTONE BULLET, PASSPORT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V602000·2016-08-15
Mercedes-Benz Recalls 2016 GLE450 for Rear Head Restraint Defect
Mercedes-Benz is recalling 2016 GLE450 vehicles because rear head restraints may not stay locked in very low temperatures, increasing injury risk in a crash.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLE450
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V596000·2016-08-12
Toyota Recalls RAV4 and Lexus HS 250h for Rear Suspension Defect
Toyota is recalling 2006-2011 RAV4 and 2010 Lexus HS 250h vehicles because improperly tightened rear suspension arms may fail, causing loss of vehicle control.
Product
TOYOTA — TOYOTA, LEXUS RAV4, HS 250 HYBRID
Category
Vehicle
Distribution
Distributed nationwide