State

Utah product recalls

72,992 recalls have nationwide distribution and so reach Utah. 4,902 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total: 4,902
Critical: 524
Severe: 1,091
Most recent: 2026-09-16

Of the 4,902 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 1,091 (22%) are Severe.

Which agencies issued them

These figures cover only the 4,902 recalls whose distribution notice names Utah specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7751–7775 of 77894

HighFDA (Devices)·Z-1218-2025·2025-03-05
Orthopedic Fixation Plates Recalled for Screw Locking Failure During Surgery
Tyber Medical is recalling 115 A.L.P.S. mvX orthopedic plates because the locking screw can pass through the locking hole during surgery, causing surgical delays and inadequate fracture fixation.
Product
A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 12H RT- Anatomic Lateral Fibula Plate, 12-Hole, Right. Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770708122 Product Description:
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1236-2025·2025-03-05
Video Colonoscope May Cause Thermal Burns to Tissue During Use
The PENTAX Medical Video Colonoscope (Model EC38-i20cL) can develop excessive heat at the tip during procedures, potentially causing thermal burns to patient tissue. Users reported dark images and steam-like smoke from the device.
Product
PENTAX Medical Video Colonoscope- Intended to provide optical visualization of (via a video monitor), and therapeutic access to the lower gastrointestinal tract Model: EC38-i20cL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1243-2025·2025-03-05
GE SIGNA MR380 NMRI System SAR Limit Exceeded During Scan Resumption
GE SIGNA MR380 NMRI systems may allow scans to resume when the 6-minute average SAR (tissue heating rate) exceeds safe limits, potentially causing excessive tissue heating especially in patients with implants or conductive contact.
Product
SIGNA MR380, NMRI system, Non-US Only
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1242-2025·2025-03-05
MRI Systems May Resume Scans When SAR Exceeds Safe Limits
Certain GE Healthcare MRI systems may incorrectly enable scan resumption when radiofrequency energy absorption exceeds FDA-set limits, potentially causing tissue heating. Risk is higher for patients with implants or touching conductive materials.
Product
SIGNA MR355, SIGNA MR360, NMRI system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1212-2025·2025-03-05
A.L.P.S. mvX Fibula Plate Recall: Locking Screw Malfunction During Surgery
Tyber Medical is recalling 408 units of the A.L.P.S. mvX Anatomic Lateral Fibula Plate because the locking screw can pass through the locking hole during surgery, causing surgical delays. No injuries have been reported.
Product
A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 6H RT: Anatomic Lateral Fibula Plate, 6-hole, Right Model/Catalog Number: 770708062
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1247-2025·2025-03-05
Leica Biosystems Cryostat CM1950 Firmware Update May Cause Tissue Loss
A software issue in the Leica Biosystems CM1950 cryostat firmware update could result in loss of patient tissue. Serial numbers 12835 and 12854 are affected.
Product
Brand Name: Leica Biosystems Cryostats Product Name: CM1950 Model/Catalog Number: 1491950C4US Software Version: firmware V3.01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1237-2025·2025-03-05
PENTAX Medical Video Upper GI Endoscope Thermal Burn Risk Recall
Pentax of America is recalling 138 PENTAX Medical Video Upper GI Scopes due to a thermal injury risk. The light guide tip can become excessively hot during endoscopic procedures, potentially burning patient tissue.
Product
PENTAX Medical Video Upper GI Scope-Intended to provide optical visualization of (via a video monitor), and therapeutic access to the lower gastrointestinal tract Model: EG29-i20c
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1241-2025·2025-03-05
GE Healthcare MRI system recalled for RF energy safety control failure
GE Healthcare's Optima MR360 MRI systems may allow unsafe RF energy exposure if a scan resumes after power loss. The user interface can incorrectly enable scanning when tissue-heating levels exceed safe limits.
Product
Optima MR360, NMRI system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1223-2025·2025-03-05
FDA Recalls Medial Tibia Plates for Intra-operative Screw Failure
Tyber Medical is recalling A.L.P.S. mvX Medial Tibia Plates due to reports that the locking screw can pass through the locking hole during surgery, causing surgical delays.
Product
A.L.P.S. mvX-MEDIAL TIBIA PLATE 12H LT-Medial Tibia Plate, 12-Hole, Left Intended forFixation of fractures of the distal tibia Model/Catalog Number: 770715121
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1208-2025·2025-03-05
Medical Imaging Software Bug Affects Diagnostic Calculations on Daylight Saving Time Dates
A software bug in IntelePACS causes incorrect diagnostic value calculations on Daylight Saving Time transition dates, risking incorrect patient diagnoses.
Product
IntelePACS (Image Fusion Module) - InteleViewer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1230-2025·2025-03-05
BD Pyxis MedBank medication cabinets recalled for operating room contraindication labeling
CareFusion is recalling BD Pyxis MedBank medication management cabinets due to inadequate labeling. A contraindication statement must be added to warn against use in procedure and operating rooms.
Product
139088-01 BD PYXIS MEDBANK MEDPASS MODULE 169-151 BD PYXIS MEDBANK MINI 1FH-2HH MEDPASS 169-152 BD PYXIS MEDBANK MINI 2HH-1FM MEDPASS 169-150 BD PYXIS MEDBANK MINI 4HH MEDPASS 169-140 BD PYXIS MEDBANK TWR MN 3FH-8HH MEDPASS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1238-2025·2025-03-05
Pentax EPK-i8020c Video Processor Recalled for Thermal Burn Risk
Pentax EPK-i8020c video processors can overheat during endoscopic procedures, creating a risk of thermal burns to patient tissues. The light guide tip becomes hot and may cause injury to mucous membranes.
Product
Pentax Medical Video Processor- Intended to be used with PENTAX Medical endoscopes, monitors and other peripheral devices for endoscopic diagnosis, treatment, and video observation. Model: EPK-i8020c
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1228-2025·2025-03-05
BD PYXIS MEDBANK Medication Systems: Labeling Update for Operating Room Restriction
CareFusion is updating labeling for BD PYXIS MEDBANK medication systems to include a contraindication against use in procedure and operating rooms. Healthcare facilities should review updated labeling and ensure appropriate device placement.
Product
155288-01 BD PYXIS MEDBANK MINI 1FH-1FM 169-137 BD PYXIS MEDBANK MINI 1FH-1FM 155311-01 BD PYXIS MEDBANK MINI 1FH-2HH 138921-01 BD PYXIS MEDBANK MINI 1HH-1FH-1HM 155159-01 BD PYXIS MEDBANK MINI 1HH-1FH-1HM 169-101 BD PYXIS MEDBANK MINI 1HH-1FH-1HM 139122-01 BD PYXIS MEDBANK MINI
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1229-2025·2025-03-05
BD PYXIS medication cabinets labeling update: operating room contraindication
CareFusion is updating labeling for BD PYXIS medication management cabinets to add a contraindication statement prohibiting use in procedure and operating rooms.
Product
139054-01 BD PYXIS MEDFLEX MN 1000 10HH-1FM 139055-01 BD PYXIS MEDFLEX MN 1000 12HH 139053-01 BD PYXIS MEDFLEX MN 1000 2HH-2FH-3FM 139041-01 BD PYXIS MEDFLEX MN 1000 2HH-2FM 139046-01 BD PYXIS MEDFLEX MN 1000 2HH-5FM 139038-01 BD PYXIS MEDFLEX MN 1000 3FM 139040-01 BD PYXIS MEDFL
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1227-2025·2025-03-05
BD PYXIS MEDBANK systems operating room contraindication labeling update
BD PYXIS MEDBANK medication management systems are subject to a labeling update adding a contraindication against use in procedure and operating rooms. Approximately 6,075 units were distributed nationwide.
Product
138913-01 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 169-114 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 138911-01 BD PYXIS MEDBANK MINI CR-4HH-P 169-115 BD PYXIS MEDBANK MINI CR-4HH-P 139001-01 BD PYXIS MEDBANK MN 200 CR-2HH-1FH-P 139002-01 BD PYXIS MEDBANK MN 200 CR-2HH-1FM-P 139000-01 BD PYXIS
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1248-2025·2025-03-05
Medical device recall: sterilization validator with incorrect incubation time
TERRAGENE S.A. is recalling 914 ASP BIOTRACE Auto Read 60 sterilization process challenge devices due to incorrect incubation time listed in the product instructions. The IFU lists 20 minutes instead of the correct 60 minutes.
Product
ASP BIOTRACE Auto Read 60 Steam BI Process Challenge Device, REF 73135.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V141000·2025-03-04
2025 Triumph Speed Twin Motorcycles Recalled for Turn Signal Visibility Defect
Triumph is recalling 2025 Speed Twin motorcycles (900, 1200, 1200 RS) due to red rear turn signals installed too close to the tail light, reducing visibility and increasing crash risk. Dealers will replace the signals with amber colored ones free of charge.
Product
TRIUMPH — TRIUMPH SPEED TWIN 1200, SPEED TWIN 1200 RS, SPEED TWIN 900
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V140000·2025-03-04
Jayco Recalls 2025 Eagle Trailers Due to Incorrect Tire Certification Labels
Jayco is recalling 2025 Eagle fifth wheels and travel trailers because certification labels contain incorrect tire load and size information.
Product
JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL, JAYCO TRAVEL TRAILER EAGLE, EAGLE HT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V138000·2025-03-03
Motiv Recalls School Buses Due to Throttle Position Sensor Defect
Motiv Power Systems is recalling certain 2017-2023 school buses because a loose throttle position sensor wire may cause a loss of drive power.
Product
MOTIV — MOTIV F-59 BEV CHASSIS SCHOOL BUS, F-53 BEV CHASSIS SCHOOL BUS, F-59 SCHOOL BUS, E-450 BEV CHASSIS SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V137000·2025-03-03
Motiv Recalls Chassis Vehicles Due to Throttle Position Sensor Defect
Motiv Power Systems is recalling specific chassis vehicles because a loose throttle position sensor pin may cause a loss of drive power, increasing crash risk.
Product
MOTIV — MOTIV F-59 BEV CHASSIS, F-53 BEV CHASSIS, E-450 CHASSIS, E-450 BEV CHASSIS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V125000·2025-02-28
Audi Q4 e-tron on-board charger failure can cut drive power
Volkswagen is recalling certain 2024-2025 Audi Q4 e-Tron and 2024 ID.4 vehicles because the on-board charger may fail and stop charging the 12-volt battery, causing a loss of drive power.
Product
AUDI — AUDI, VOLKSWAGEN Q4 E-TRON, Q4 SPORTBACK E-TRON, ID.4
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V132000·2025-02-28
Ford trucks may fail to apply electric trailer brakes
Ford is recalling certain 2021-2022 F-150, 2022 Maverick, Expedition, Navigator and Super Duty vehicles previously repaired under 22V-193, because a towed trailer's electric brakes may not apply.
Product
FORD — FORD, LINCOLN F-150, MAVERICK, EXPEDITION, NAVIGATOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V127000·2025-02-28
Ford Maverick control modules may miss a low 12-volt battery
Ford is recalling certain 2022 Maverick vehicles previously repaired under 24V-590, because the body and powertrain control modules may fail to detect a change in 12-volt battery state of charge.
Product
FORD — FORD MAVERICK
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V126000·2025-02-28
Ford EcoSport front half shafts can disconnect from the transmission
Ford is recalling certain 2021-2022 EcoSport vehicles because the front axle half shafts may disconnect from the transmission, causing a loss of drive power and a possible rollaway.
Product
FORD — FORD ECOSPORT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V135000·2025-02-28
Mercedes Sprinter parking brake bracket welds can fail causing rollaway
Daimler Vans is recalling certain 2024 Mercedes-Benz Sprinter vehicles because the parking brake cable bracket welds may fail and disengage the parking brake, failing FMVSS 105.
Product
MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 2500, SPRINTER 1500, SPRINTER 4500, SPRINTER 3500
Category
Vehicle
Distribution
Distributed nationwide