State

Utah product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45626–45650 of 78740

HighFDA (Devices)·Z-2732-2017·2017-07-19
Nova Biomedical Stat Profile Prime Analyzer Software Recall
Nova Biomedical is recalling Stat Profile Prime Analyzers because a software defect could cause scheduled quality control tests to overwrite pending patient results.
Product
Nova Biomedical Stat Profile Prime Analyzer as follows: PN 52855 Stat Profile Prime ABG Analyzer PN 53655 Stat Profile Prime ABG Analyzer with Scanner PN 52856 Stat Profile Prime CCS Analyzer PN 53656 Stat Profile Prime CCS Analyzer with Scanner PN 53657 Stat Profile Prime…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2693-2017·2017-07-19
St. Jude Medical Recalls Infinity 5 Implantable Pulse Generators
St. Jude Medical is recalling 443 Infinity 5 Implantable Pulse Generators due to a risk of losing neuromodulation therapy when exposed to monopolar electrosurgical devices.
Product
Infinity 5, Implantable Pulse Generator, REF 6660, Rx only, STERILE EO, Product Usage: The Infinity IPG is an electronic device designed to be connected to one or two extensions. It is powered by a hermetically sealed battery within a titanium case and uses microelectronic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2574-2017·2017-07-19
Recall of 365 Everyday Value Precooked Breaded Fish Squares for Undeclared Milk
National Fish & Seafood, Inc. is recalling 365 Everyday Value Precooked Breaded Fish Squares because the product may contain undeclared milk.
Product
365 EVERYDAY VALUE ALL NATURAL PRECOOKED BREADED FISH SQUARES 10/2 LBS NET WT. 20 LBS (9.07 kg)
Category
Food
Distribution
24 states
HighFDA (Devices)·Z-2683-2017·2017-07-19
ICU Plum A+ Infusion Systems Recalled for Battery-Related Therapy Interruption
ICU is recalling 363,892 Plum A+ Infusion Systems because battery issues can cause an E321 error code, potentially interrupting patient therapy.
Product
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2710-2017·2017-07-19
Toshiba APLIO 300 Ultrasound Systems Recalled for Incorrect Velocity Trace Display
Toshiba is recalling 90 APLIO 300 diagnostic ultrasound systems because they may display incorrect velocity trace values when using the Continuous Trace method.
Product
APLIO 300 TUS-A300 diagnostic ultrasound system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2549-2017·2017-07-19
Matlaws Pre-Cooked Fish Squares Recalled for Undeclared Milk
National Fish & Seafood is recalling Matlaws All Natural Panko Pre-Cooked Fish Squares because the product may contain undeclared milk.
Product
MATLAWS ALL NATURAL PANKO PRE COOKED FISH SQUARES 10 LB and 10/2 LB
Category
Food
Distribution
24 states
HighFDA (Devices)·Z-2692-2017·2017-07-19
St. Jude Medical Recalls Proclaim 7 Elite Implantable Pulse Generators
St. Jude Medical is recalling 9,529 Proclaim 7 Elite implantable pulse generators due to a risk of losing neuromodulation therapy when exposed to monopolar electrosurgical devices.
Product
Proclaim 7 Elite, Implantable Pulse Generator, REF 3662, Rx only, STERILE EO Product Usage: The Proclaim implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2712-2017·2017-07-19
Toshiba APLIO i-series Ultrasound Systems Recalled for Incorrect Velocity Readings
Toshiba is recalling 28 APLIO i-series diagnostic ultrasound systems because they may display incorrect velocity values when using the Continuous Trace method.
Product
APLIO i-series: a) APLIO i700 TUS AI700 b) APLIO i800 TUS AI800 diagnostic ultrasound system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2714-2017·2017-07-19
ArjoHuntleigh Flowtron ACS900 Medical Pump Recalled for Deflation Failure
Arjo, Inc. is recalling 40,675 Flowtron ACS900 medical pumps worldwide because the device may fail to deflate the calf garment as intended without triggering an alarm.
Product
ArjoHuntleigh Flowtron ACS900, medical pump, software V1.099 Device is used to prevent the occurrence of Deep Vein Thrombosis (DVT) in at-risk patients. The system must be used as part of a prescribed plan of car under the supervision of trained medical and/or Clinical staff.…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2550-2017·2017-07-19
Matlaws Pre-Cooked Fish Sticks Recalled for Undeclared Milk
National Fish & Seafood, Inc. is recalling Matlaws All Natural Panko Pre-Cooked Fish Sticks because the product may contain undeclared milk.
Product
MATLAWS ALL NATURAL PANKO PRE COOKED FISH STICKS 1/10 LB and 10/2 LB
Category
Food
Distribution
24 states
HighFDA (Devices)·Z-2727-2017·2017-07-19
Natus Neurology Recalls Elite Obstetric Probes Due to Excessive Background Noise
Natus Neurology is recalling 2,335 Elite Obstetric probes because excessive background noise may mask fetal heart rate and blood flow monitoring.
Product
Nicolet¿ Elite¿ 2 MHz OB Water Proof Probe, Model #: X1L008, Catalog Code: NW20. Intended for non-invasive support, i.e. early detection of fetal life, monitor blood flow before and after surgery, etc.
Category
Medical Device
Distribution
44 states
HighFDA (Food)·F-2588-2017·2017-07-19
NatureBox Mini Crispy Snickerdoodles Recalled for Cashew Fragment
NatureBox is recalling Mini Crispy Snickerdoodles because a cashew fragment was found during packing, posing a potential allergen risk.
Product
NatureBox Mini Crispy Snickerdoodles: Cinnamon-sugar cookies made with whole wheat. Contains: Wheat, Milk and Egg.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2463-2017·2017-07-19
3CS Organics Recalls HIPP Infant Formula Due to Labeling Issues
3CS Organics LLC is recalling HIPP infant formula products because they are not FDA approved and lack full English labeling.
Product
HIPP HA Combiotik HA 1, 500g (4/case), HIPP Combiotik HA 2, 500g (4/case), HA Combiotik Pre HA, 500g (4/case), HIPP Combiotic Growing Up Milk 3, 600g (4bx/case)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2711-2017·2017-07-19
Toshiba APLIO 500 Ultrasound Systems Recalled for Incorrect Velocity Trace Values
Toshiba American Medical Systems Inc. is recalling 307 APLIO 500 diagnostic ultrasound systems because they may display incorrect values when using the Continuous Trace method on Spectral Doppler.
Product
APLIO 500 TUS-A500 diagnostic ultrasound system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2380-2017·2017-07-19
Source Naturals Hydrogen Boost Capsules Recalled for Undeclared Boron
Source Naturals Hydrogen Boost Capsules are being recalled because they contain low levels of undeclared boron. The recall covers 55,354 units distributed nationwide.
Product
Source Naturals Hydrogen Boost Capsule: 6 Count Trial, 30 Count, 60 Count; Ingredient: Maltodextrin, Cellulose (Capsules, Silica and magnesium stearate; 30 count Bottle - Product SN1855: 60 count Bottle - Product SN1856; 6 count Bottle - Product SN2314; 30 count + 30…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2464-2017·2017-07-19
3CS Organics Recalls HIPP Organic Infant Milk Products for Labeling Issues
3CS Organics is recalling HIPP Organic infant milk products because they are not FDA approved and lack full English labeling.
Product
HIPP Organic Comb Hungry Infant Milk, 800g (4bx/case), HIPP Organic Comb First Infant Milk, 800g (4bx/case), HIPP Organic Combiotic Follow on Milk 2, 800g (4bx/case), HIPP Organic Good Night Milk from 6 Months, 350g (12cans/case)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2465-2017·2017-07-19
HIPP Infant Formula Recalled for Lack of FDA Approval and English Labels
3CS Organics LLC is recalling HIPP infant formula products because they are not FDA approved and lack complete English labeling.
Product
HIPP Tetrapack-Liquid , Single Serve Combiotik Hungry Infant, 200mL (6pk/24cases), HIPP Tetrapak-Liquid, Single Serve Combiotik First Infant Milk, 200mL (6pk/case)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2708-2017·2017-07-19
Toshiba XARIO 100 Ultrasound Systems Recalled for Incorrect Velocity Readings
Toshiba American Medical Systems is recalling seven XARIO 100 diagnostic ultrasound systems because they may display incorrect values when using the Continuous Trace method for velocity measurements.
Product
XARIO 100 TUS-X100 diagnostic ultrasound system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2469-2017·2017-07-19
3CS Organics Recalls Topfer Lactana Bio Infant Formula for Labeling Issues
3CS Organics LLC is recalling Topfer Lactana Bio infant and follow-up formula because the product is not FDA approved and lacks complete English labeling.
Product
Topfer Lactana Bio 1 Anfangsmilch, 600g (3/case), Topfer Lactana Bio 2, Bio Folgemilch, 600g (3bx/case)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2462-2017·2017-07-19
3CS Organics Recalls HIPP Bio Combiotik Infant Formula for Labeling Issues
3CS Organics LLC is recalling HIPP Bio Combiotik infant formula products because they are not FDA approved and not all products are labeled in English.
Product
HIPP Bio Combiotik 1, Canister, 900g (4/case), HIPP Bio Combiotik 2, Canister, 900g (4/case), HIPP Bio Combiotik 3, Canister, 900g (4/case), HIPP Bio Combiotik 1, 600g (4bx/case), HIPP Bio Combiotik 2, 600g (4bx/case), HIPP Bio Combiotik 3, 600g (4/case), HIPP Bio Compiotik…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2467-2017·2017-07-19
HOLLE Organic Infant Formula Recalled for Lack of FDA Approval
3CS Organics LLC is recalling HOLLE organic infant formula products because they are not FDA approved and lack English labeling.
Product
HOLLE Bio Zulgelingen Opvolgmelk 2, (3/case), HOLLE Bio Lait de suite, 2, 400g (6/case), HOLLE Bio Lait pour Nourrissons Zulgelingenmelk, 400g (6/case), HOLLE Lait Pour Nourrissons 1er Age Bio, 400g (6/case). HOLLE Bio Lait de Suit Au Lait De Chevre, 400g (6/case) , HOLLE…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2730-2017·2017-07-19
Beckman Coulter Synchron AQUA CAL Level 1 Calibration Kits Recalled
Beckman Coulter is recalling Synchron AQUA CAL Level 1 kits due to a sodium recovery shift that may affect system calibration.
Product
Beckman Coulter Synchron AQUA CAL Level 1, Part No. 471288 Product Usage: Used for the system calibration of Na, K, Cl, Urea N, Urea, Glucose Creatine, Ca, CO2, and P in UniCel DxC Systems.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2383-2017·2017-07-19
Source Naturals Renewal Antioxidant Tablets Recalled for Undeclared Boron
Threshold Enterprises Ltd is recalling Source Naturals Renewal Antioxidant Tablets because they contain low levels of undeclared boron.
Product
Source Naturals Renewal Antioxidant Tablet: 10 Count Sample Pack, 30 Count, 60 Count, & 120 Count per bottle; Ingredient: Maltodextrin, Cellulose (Capsules, Silica and magnesium stearate; 30 count Bottle - Product SN1750: 60 count Bottle - Product SN1751; 120 count…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2461-2017·2017-07-19
HIPP Anti-Reflux Infant Formula Recalled for Lack of FDA Approval
3CS ORGANICS LLC is recalling HIPP Anti-Reflux AR Bio-Spezialnahrung because the product is not FDA approved and lacks complete English labeling.
Product
HIPP Anti-Reflux AR Bio-Spezialnahrung, 500g (4/case)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2715-2017·2017-07-19
CryoLife On-X Prosthetic Heart Valve Recall for Incorrect Labeling
CryoLife, Inc. is recalling 52 On-X Prosthetic Heart Valves because the sewing ring type was mislabeled as Standard instead of Anatomic.
Product
On-X Prosthetic Heart Valve Product Usage: Indicated for the replacement of diseased, damaged, or malfunctioning native or prosthetic heart valves in the aortic and mitral positions
Category
Medical Device
Distribution
Distributed nationwide