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.

40301–40325 of 78725

ModerateFDA (Devices)·Z-2652-2018·2018-08-15
ICU Medical Recalls Blood Sets with Inaccurate DEHP Labeling
ICU Medical is recalling specific blood tubing sets because they were labeled as not containing DEHP, even though the product may contain small amounts of the chemical.
Product
125" (318 cm) Y-Type Blood Set w/170 Micron Filter, Hand Pump, 3 Clave¿, Remv 3 Gang 4-Way Stopcock w/Baseplate, Rotating Luer, 3 Ext, Sterile The blood tubing accessory with CLAVE Connector is a single use, sterile, non-pyrogenic device intended for use as an adjunct to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2648-2018·2018-08-15
ICU Medical Recalls Blood Sets with Incorrect DEHP Labeling
ICU Medical is recalling specific blood sets labeled as DEHP-free because they may contain small amounts of DEHP.
Product
143" (363 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter, Hand Pump, 2 Clave¿, Drop-In Ext w/3 Gang 4 Way Stopcocks, MicroClave¿, Luer Lock, Sterile The blood tubing accessory with CLAVE Connector is a single use, sterile, non-pyrogenic device intended for use as an adjunct…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2615-2018·2018-08-15
ICU Medical Recalls Blood Sets with Incorrect DEHP Labeling
ICU Medical is recalling 160,016 blood sets labeled as DEHP-free because they may contain small amounts of DEHP.
Product
112" Y-Type Blood Set w/170 Micron Filter, Hand Pump, Pre-Slit Port, Rotating Luer, Sterile The blood tubing accessory with CLAVE Connector is a single use, sterile, non-pyrogenic device intended for use as an adjunct to blood tubing sets or venipuncture devices for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2639-2018·2018-08-15
ICU Medical Recalls Blood Sets with Incorrect DEHP Labeling
ICU Medical is recalling 160,016 blood sets because some were labeled as not containing DEHP, even though the product may contain small amounts of the chemical.
Product
128" (325 cm) Y-Type Blood Set with 170 Micron Filter, Hand Pump, 2 Clave¿, Removable 2 Gang (Blue, Yellow) 1o2¿ Manifold, Baseplate, 1 Ext, Rotating Luer, Sterile The blood tubing accessory with CLAVE Connector is a single use, sterile, non-pyrogenic device intended for use…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2657-2018·2018-08-15
ICU Medical Recalls Blood Sets With Incorrect DEHP Labeling
ICU Medical is recalling 116-inch Y-Type Blood Sets because they were labeled as not containing DEHP, even though the product may contain small amounts of the chemical.
Product
116" (295 cm) Y-Type Blood Set w/170 Micron Filter, Hand Pump, 3 MicroClave¿, 2 Ext, Rotating Luer, Sterile The blood tubing accessory with CLAVE Connector is a single use, sterile, non-pyrogenic device intended for use as an adjunct to blood tubing sets or venipuncture…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2641-2018·2018-08-15
ICU Medical Recalls Blood Sets With Incorrect DEHP Labeling
ICU Medical is recalling specific blood tubing sets labeled as DEHP-free that may contain small amounts of the chemical.
Product
88" (224 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter, Hand Pump, Clave¿, Rotating Luer w/Filter Cap, Sterile The blood tubing accessory with CLAVE Connector is a single use, sterile, non-pyrogenic device intended for use as an adjunct to blood tubing sets or venipuncture…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1035-2018·2018-08-15
Baxter Recalls Levofloxacin Injection Due to High Potency Levels
Baxter Healthcare is recalling specific lots of Levofloxacin Injection in 5% Dextrose because the solution concentration was higher than specified.
Product
LEVOFLOXACIN — LEVOFLOXACIN (LEVOFLOXACIN)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Food)·F-1768-2018·2018-08-15
Kraft Heinz Recalls Asian Style Sesame Ginger Dressing Due to Spoilage
Kraft Heinz is recalling 19,560 cases of Food Network Kitchen Inspirations Asian Style Sesame Ginger Dressing due to premature spoilage caused by lactic acid producing bacteria.
Product
Food Network Kitchen Inspirations Asian Style Sesame Ginger Dressing. 12 oz glass bottle, 6 bottles per case Shelf Stable and Refrigerate After Opening UPC 0021000068876
Category
Food
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1041-2018·2018-08-15
Valeant Recalls Diazepam Rectal Gel Due to Missing Lot and Expiration Dates
Valeant Pharmaceuticals is recalling 306 cartons of Diazepam Rectal Gel because the outer cartons are missing lot numbers and expiration dates.
Product
DIAZEPAM — DIAZEPAM (DIAZEPAM)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1047-2018·2018-08-15
Right Value Drug Stores Recalls Testosterone Pellets Due to Labeling Error
Right Value Drug Stores is recalling 4,800 Testosterone 200 mg Pellets because the label contains an incorrect expiration date.
Product
Testosterone 200 mg Pellet, Rx only, Carie Boyd's Prescription Shop 122 Grapevine Hwy., Hurst, TX 76054, 800-930-4361
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·18E082000·2018-08-14
Akoury Recalls AK88S Motorcycle Helmets for Impact Protection Defect
Akoury is recalling AK88S motorcycle helmets because they may not adequately protect the wearer in a crash, increasing the risk of injury.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·18204·2018-08-14
Koehler-Bright Star Recalls WorkSafe Flashlights Due to Explosion Hazard
Koehler-Bright Star is recalling about 7,500 WorkSafe 3-D cell flashlights because a missing circuit board component poses an explosion hazard.
Product
WorkSafe 3-D cell flashlights
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·18V529000·2018-08-13
Roadtrek Zion Motorhomes Recalled for Rear Brake Line Damage Risk
Erwin Hymer is recalling 2015-2018 Roadtrek Zion motorhomes because sofa installation may have damaged the rear brake line, increasing stopping distance and crash risk.
Product
ROADTREK — ROADTREK ZION
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V528000·2018-08-13
Roadtrek Motorhomes Recalled for Potential Diesel Fuel Tank Damage
Erwin Hymer is recalling 2017-2018 Roadtrek motorhomes because the diesel fuel tank may have been damaged during seat installation, increasing fire risk.
Product
ROADTREK — ROADTREK E-TREK, RS ADVENTUROUS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V527000·2018-08-13
Forest River Recalls Recreational Trailers Due to Awning Deployment Risk
Forest River is recalling specific 2018-2019 recreational trailers because the awning may deploy while moving, increasing the risk of a crash.
Product
FOREST RIVER — FOREST RIVER, COACHMEN ROCKWOOD, ADRENALINE, FORESTER, XLR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18E081000·2018-08-10
Cummins Recalls Diesel Engines Due to Fuel Line Burst Risk
Cummins is recalling ISX15 and X15 diesel engines because a restricted fuel pump screen can cause the nylon fuel line to burst, leading to fuel leaks or engine stalling.
Product
FUEL SYSTEM, OTHER:DELIVERY:FUEL PUMP recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V526000·2018-08-10
KZRV Sportsmen Travel Trailers Recalled for Propane Line Fire Risk
KZRV is recalling 2018-2019 Sportsmen 333BHK travel trailers because liquid propane lines routed through the wheel well may be damaged by road debris, increasing fire risk.
Product
KZRV — KZRV SPORTSMEN
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18E080000·2018-08-09
TRW Recalls Outer Tie Rods for Loss of Steering Risk
TRW is recalling specific outer tie rods sold as replacement parts for 1988-2000 GM vehicles because the locking nut may fail, causing a loss of steering.
Product
STEERING:LINKAGES:TIE ROD ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V525000·2018-08-09
Freightliner Trucks Recalled for Insufficiently Tightened Brake Caliper Bolts
Daimler Trucks North America is recalling 2018-2019 Freightliner trucks because brake caliper mounting bolts may be loose, which can reduce braking effectiveness and increase crash risk.
Product
FREIGHTLINER — FREIGHTLINER 108SD, 114SD, CASCADIA, 122SD
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V523000·2018-08-09
Chrysler Recalls 2018-2019 Vehicles for Rear Brake Caliper Coating Defect
Chrysler is recalling specific 2018-2019 Dodge and Jeep vehicles because rear brake caliper pistons may have insufficient coating, potentially reducing braking performance.
Product
DODGE — DODGE, JEEP GRAND CARAVAN, CHEROKEE, JOURNEY, COMPASS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V524000·2018-08-09
Chrysler, Jeep, and Ram Vehicles Recalled for Powertrain Control Module Defect
FCA US LLC is recalling specific 2017-2019 Chrysler, Jeep, Ram, Dodge, and Fiat vehicles because a faulty voltage regulator chip may cause the vehicle to stall or fail to start.
Product
CHRYSLER — CHRYSLER, RAM, JEEP PACIFICA PLUG-IN HYBRID, PACIFICA, 1500, RENEGADE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·18203·2018-08-09
Harbor Freight Recalls Electronic Handgun Safes Due to Serious Injury Hazard
Harbor Freight Tools is recalling about 25,000 electronic handgun safes because they can open upon impact, posing a serious injury risk to children.
Product
Electronic handgun safes
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·18202·2018-08-09
Vitamix Recalls Ascent and Venturist Blending Containers Due to Laceration Hazard
Vitamix is recalling Ascent and Venturist series blending containers because they can separate from the blade base, exposing blades and posing a laceration hazard.
Product
Ascent™ and Venturist™ Series 8-ounce and 20-ounce blending containers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·18V511000·2018-08-09
Gillig Recalls Low Floor Buses Due to Turn Signal Flashing Defect
Gillig is recalling 2012-2018 Low Floor buses because front and rear turn signals may flash at different rates, potentially confusing other drivers.
Product
GILLIG — GILLIG LOW FLOOR
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1675-2018·2018-08-08
Probiotic Supplement Recalled for Potential Undeclared Allergens
LL'S Magnetic Clay Inc. is recalling Prescript-Assist Probiotic & Prebiotic supplements because they may contain undeclared almonds, shellfish, milk, eggs, or peanuts.
Product
Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary Supplement, 60-capsule or 90-capsule bottles; UPC Codes: 853956003157, 853956003539
Category
Food
Distribution
Distributed nationwide