State

Utah product recalls

73,092 recalls have nationwide distribution and so reach Utah. 4,905 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total: 4,905
Critical: 524
Severe: 1,093
Most recent: 2026-09-23

Of the 4,905 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 1,093 (22%) are Severe.

Which agencies issued them

These figures cover only the 4,905 recalls whose distribution notice names Utah specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8276–8300 of 77997

HighFDA (Devices)·Z-1058-2025·2025-02-05
Karl Storz Uretero-Renoscope recalled for unapproved reprocessing instructions
Karl Storz Endoskope Uretero-Renoscope (Model 27011L) is recalled due to Instructions for Use containing reprocessing procedures that have not been FDA-reviewed or approved. The recall affects 5 units distributed nationwide.
Product
KARL STORZ - ENDOSKOPE, REF: 27011L, Uretero-Renoscope, 8 Fr., 6¿, 43cm, NON STERILE, RxONLY, CE 0123
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1025-2025·2025-02-05
AXIOS Stent Delivery System: Detaching Outer Sheath May Prevent Stent Expansion
Boston Scientific is recalling 1,144 AXIOS Stent Delivery System units because the outer sheath's distal black tip can detach. If this occurs, the tip may remain around the stent saddle and prevent proper stent expansion, requiring device exchange.
Product
AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN: M00553650
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1065-2025·2025-02-05
Alphatec Calibrate CCX Interbody Implants Recalled for Post-Operative Collapse
Alphatec Spine is recalling Calibrate CCX spinal implants used in fusion procedures after receiving complaints of post-operative implant collapse. Approximately 1,511 implants were distributed nationwide.
Product
Calibrate CCX Interbody System for spinal fusion procedures: Implants: (1) Calibrate CCX-O, 7 x 10 x 25mm 5 degrees, Part #325-07102505, nonsterile; (2) Calibrate CCX-O, 7 x 10 x 25mm 10 degrees, Part #325-07102510, nonsterile; (3) Calibrate CCX-O, 7 x 10 x 25mm 15 d
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1030-2025·2025-02-05
AXIOS Stent and Delivery System Recalled for Improper Expansion Risk
The AXIOS Stent and Delivery System is being recalled because the outer sheath can detach and prevent proper stent expansion, requiring device replacement during the procedure.
Product
AXIOS Stent and Delivery System 10mmx10mm UPN: M00553740
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1062-2025·2025-02-05
Karl Storz Ureteroscope Model 27001K Recalled for Unapproved Reprocessing Instructions
Karl Storz is recalling its Ureteroscope (Model 27001K) because the Instructions for Use contain reprocessing procedures that have not been reviewed or approved by the FDA. All 185 units distributed nationwide are affected.
Product
KARL STORZ - ENDOSKOPE, REF: 27001K, Ureteroscope, 9.5 Fr., 6¿, 34 cm, NON STERILE, RxONLY, CE 0123
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1022-2025·2025-02-05
Medtronic Percutaneous Reference Pins May Not Fit Properly
Medtronic is recalling sterile percutaneous reference pins used in image-guided surgery because the pins may not fit into the patient reference frame or adapter, potentially affecting proper surgical tracking.
Product
Medtronic PIN, 100mm STERILE PERCUTANEOUS REF: 9733235 Medtronic PIN, 150MM, STERILE PERCUTANEOUS REF: 97733236 The Sterile Percutaneous Reference Pin Set is intended to be used to place and remove a pin percutaneously into bony patient anatomy for rigid attachment of a pat
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0455-2025·2025-02-05
Alpha Test supplement capsules recalled for unapproved cathine ingredient
Iovate Health Sciences is recalling Alpha Test 120-count capsules containing cathine, an unapproved ingredient not permitted in dietary supplements. Affected products were distributed across the United States and internationally.
Product
Alpha Test 120 count Black labeled plastic bottle, 12 bottles per case of 120 count capsules each per bottle, Store in a cool, dry place (60 F to 80 F), UPC 6-31656-60676-8, SKU0001191, SKU0002075
Category
Drug
Distribution
30 states
HighFDA (Devices)·Z-1053-2025·2025-02-05
Karl Storz Pediatric Cysto-Urethroscope Recalled for Unapproved Reprocessing Instructions
Karl Storz is recalling 185 Pediatric Cysto-Urethroscope instruments nationwide. The product instructions contain reprocessing methods that have not been reviewed or approved by the FDA for safety and effectiveness.
Product
KARL STORZ - ENDOSKOPE, REF: 27030KB, Pediatric Cysto-Urethroscope, NON STERILE, CE
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1039-2025·2025-02-05
Knee Implant Component Recalled for Incorrect Metal Post Assembly
Zimmer, Inc. is recalling 155 units of NexGen LCCK Legacy knee implant components because the metal support post was assembled incorrectly in some units. The defective assembly could compromise implant function.
Product
NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Yellow/E,F - Height 10 mm, Item Number 00-5994-032-10
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V056000·2025-02-05
2025 Honda Pilot third-row seat belt may not restrain occupant
Honda is recalling certain 2025 Pilot vehicles because the third-row passenger seat belt may not function due to incorrect routing. A non-functioning seat belt cannot properly restrain occupants, increasing injury risk during a crash.
Product
HONDA — HONDA PILOT
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1042-2025·2025-02-05
Medline procedure kits recalled for surgical mask bioburden contamination risk
Medline procedure kits containing surgical masks are recalled nationwide because included masks failed to meet bioburden testing standards, creating potential infection risk during medical procedures.
Product
Medline procedure kits labeled as: 1) CENTRAL LINE DRESSING KIT, Reorder number DYNDC3189; dressing change tray
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1024-2025·2025-02-05
AXIOS Stent Delivery System Outer Sheath May Detach During Deployment
Boston Scientific's AXIOS Stent Delivery System is being recalled because the outer sheath can detach during use, preventing proper stent expansion and requiring device exchange.
Product
AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm UPN: M00553640
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1063-2025·2025-02-05
Karl Storz Ureteroscope Recalled for Unapproved Reprocessing Instructions
Karl Storz is recalling 180 ureteroscopes due to instructions for use containing reprocessing procedures that have not been reviewed or approved by the FDA.
Product
KARL STORZ - ENDOSKOPE, REF: 27002K, Ureteroscope, 9.5 Fr., 6¿, 34 cm, NON STERILE, RxONLY, CE 0123
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0209-2025·2025-02-05
Badger 50 Mineral Sunscreen Recalled for Missing Drug Facts Labeling
The W.S. Badger Company is recalling Badger 50 mineral sunscreen tins lacking the complete drug facts label, barcode, and directions for use. The recall affects 4,834 tins distributed nationwide.
Product
BADGER 50, ADVENTURE SPORT MINERAL SUNSCREEN WITH CLEAR ZINC, (uncoated 25% zinc oxide), 2.4 oz., Tin, W.S. Badger Company, Inc, 768 Route 10, Gilsum NH, 03448 UPC 6 34084 47150 2
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·25V054000·2025-02-04
Highland Ridge Recalls 2025 Open Range 3X Trailers for Incorrect Tire Labeling
Highland Ridge RV is recalling 2025 Open Range 3X fifth-wheel travel trailers because the vehicle certification label lists the wrong tire size, which could lead to incorrect tire installation.
Product
HIGHLAND RIDGE FW — HIGHLAND RIDGE FW OPEN RANGE 3X
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V053000·2025-02-03
New Flyer Transit Buses Recalled for Fuel Hose Separation Risk
New Flyer is recalling 210 transit buses because fuel filter hoses may separate, causing leaks, engine stalls, and fire risks.
Product
NEW FLYER — NEW FLYER XDE60, XD35, XD40, XD60
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V052000·2025-02-03
Temsa Recalls 2024 TS35 Vehicles Due to Fuel Hose Separation Risk
Temsa is recalling 2024 TS35 vehicles with Cummins L9 engines because fuel filter hoses may separate, causing leaks, engine stalls, and fire or crash risks.
Product
TEMSA — TEMSA TS35
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V048000·2025-01-31
Ford and Lincoln rearview cameras may show blank or distorted images
Ford is recalling certain 2021 Expedition, 2021-2022 Super Duty F-250 to F-600 and 2020-2022 Lincoln Corsair vehicles because the rearview camera may display a blank or distorted image.
Product
FORD — FORD, LINCOLN F-250 SD, F-550 SD, F-450 SD, F-350 SD
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V051000·2025-01-31
Roadtrek Recalls Westfalia Wave Vans Due to Incorrect Weight Labels
Roadtrek is recalling 2023-2025 Westfalia Wave Pop Top vans because incorrect weight labels may lead to unintentional overloading and increased crash risk.
Product
ROADTREK — ROADTREK WESTFALIA WAVE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V049000·2025-01-31
Ford Recalls 2025 Models for Instrument Panel Illumination Defect
Ford is recalling 2025 Bronco Sport, Escape, and Lincoln Corsair vehicles because the instrument panel may fail to illuminate, increasing crash risk.
Product
FORD — FORD, LINCOLN BRONCO SPORT, ESCAPE, CORSAIR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V045000·2025-01-30
Autocar Recalls 2023-2025 E-ACTT Vehicles Due to Software Error
Autocar is recalling 2023-2025 E-ACTT vehicles because a software error may cause the vehicle to roll away on an incline or stall the engine.
Product
AUTOCAR — AUTOCAR E-ACTT
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·25114·2025-01-30
Portable Folding Stadium Seats Recalled Due to Fall and Injury Hazards
AMX Global is recalling about 22,500 portable folding stadium seats because security hooks can crack and break, posing fall and injury risks. The company received reports of hook failures including falls and an injury.
Product
AMX Global Portable Folding Stadium Seats
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25113·2025-01-30
Girls pajamas recalled due to flammability regulation violation, burn-injury risk
Cozchique, Tebbis, and Beeziac girls pajamas sold on Amazon violate federal flammability regulations for children's sleepwear, posing a risk of burn injuries. About 6,050 units distributed May through September 2024.
Product
Cozchique, Tebbis and Beeziac Girls Pajamas
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25109·2025-01-30
Matrix-brand Training Cycles Recalled Due to Unexpected Seat Collapse
Johnson Health Tech North America is recalling approximately 12,885 Matrix-brand Training Cycles due to seats that can unexpectedly lower during use. The company received 63 reports, including two falls, but no injuries have been reported.
Product
Matrix-brand Training Cycles
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25110·2025-01-30
Cabinet Health 4 oz. Refillable Medicine Bottles Recalled for Degrading Lids
Cabinet Health is recalling about 65,000 refillable 4 oz. medicine bottles. The plastic lids can degrade with repeated use, losing child-resistance and posing a poisoning risk if children access the contents.
Product
Cabinet Health 4 oz. Refillable Medicine Bottles
Category
Consumer Product
Distribution
Distributed nationwide