State

Utah product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50076–50100 of 78743

SevereFDA (Food)·F-2402-2016·2016-10-05
Bounce Apple Cinnamon Protein Energy Balls Recalled for Listeria Risk
Bounce Life Style HQ is recalling Apple Cinnamon Protein Energy Balls due to potential Listeria monocytogenes contamination from sunflower kernels.
Product
US - Bounce Apple Cinnamon Protein Punch Energy Balls (old name), net wt. 1.48 oz. (42g). Product UPC Codes are 852949003723 (individual packs) and 852949003730 (12-unit boxes). US - Bounce Apple Cinnamon Protein Energy Balls (new name), net wt. 1.48 oz. (42g). Product UPC…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2883-2016·2016-10-05
Trividia TRUEread Blood Glucose Test Strips Recalled for Incorrect Low Readings
Trividia Health is recalling TRUEread Blood Glucose Test Strips because they may provide incorrect low blood glucose levels.
Product
TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with TRUEresult and TRUE2go meters. TRUEread Blood Glucose Test Strips are available in vials with 10 ct., 25 ct., 50 ct., and sold as 10 ct. with meters. Quantitatively measure whole blood glucose in a…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2880-2016·2016-10-05
Trividia Health Recalls TRUEread Blood Glucose Test Strips for Incorrect Readings
Trividia Health is recalling TRUEread Blood Glucose Test Strips because they may provide incorrect low blood glucose levels, potentially affecting patient safety.
Product
TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with TRUEresult and TRUE2go meters. TRUEread Blood Glucose Test Strips are available in vials with 10 ct., 25 ct., 50 ct., and sold as 10 ct. with meters. Quantitatively measure whole blood glucose in a…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2784-2016·2016-10-05
Anspach Effort Recalls Small Battery Drive Adaptors Due to Burst Risk
The Anspach Effort, Inc. is recalling 1,833 Small Battery Drive adaptors worldwide because they may generate excessive internal pressure and burst.
Product
Adaptor for Small Battery Drive and Small Battery Drive II. Product Usage: The Light Adaptor for Small Battery Drive (SBD) /Small Battery Drive II (SBD II) is designed for use in traumatology and orthopedic surgery of the skeleton, i.e. drilling, reaming or cutting bone. The…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-2603-2016·2016-10-05
Meadow Gold Dairy Half & Half Recalled for Insufficient Pasteurization
Dean Foods is recalling Meadow Gold Dairy Pure Fresh Half & Half due to insufficient pasteurization. The product was distributed in Idaho, Oregon, Wyoming, and Utah.
Product
Meadow Gold Dairy Pure Fresh Half & Half One Quart (946 mL)
Category
Food
Distribution
4 states
SevereNHTSA·16V712000·2016-10-05
Daimler Recalls 2017 Thomas Built Buses Saf-T-Liner C2 School Bus Chassis
Daimler Trucks North America is recalling 162 model year 2017 Thomas Built Buses Saf-T-Liner C2 school bus chassis because the brake transmission shift interlock may be inoperable.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V709000·2016-10-05
NHTSA Recalls 2015-2016 Wells Cargo and Haulmark Snowmobile Trailers
Universal Trailer Cargo Group is recalling 89 aluminum snowmobile trailers because cross winds may cause them to tip or lift, potentially tearing the couplers.
Product
WELLS CARGO — WELLS CARGO, HAULMARK ALUMINUM SNOWMOBILE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-2605-2016·2016-10-05
Dean Foods Recalls Old Style Meadow Gold Heavy Whipping Cream
Dean Foods is recalling 60 pints of Old Style Meadow Gold Heavy Whipping Cream due to insufficient pasteurization. The product was distributed in Idaho, Oregon, Wyoming, and Utah.
Product
Old Style Meadow Gold Heavy Whipping Cream Grade A Pint (473 mL) in waxed cardboard container
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-2896-2016·2016-10-05
Zyno Medical Administration Set Recalled for Potential Filter Leaking
Zyno Medical LLC is recalling 47,989 sterile administration sets due to a potential filter leaking defect. The sets are used to administer fluids to patients.
Product
Zyno Medical Administration Set Sterile. Rx For Use with Zyno Medical Infusion Pumps or Gravity Feed Product Code: B2-70072-F Product Usage: Zyno Medical Administration Set is a device used to administer fluids from a container to a patients vascular system through a needle…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2882-2016·2016-10-05
Trividia Health Recalls TRUEread Blood Glucose Test Strips for Inaccurate Readings
Trividia Health is recalling TRUEread Blood Glucose Test Strips because they may provide incorrect low blood glucose levels. The recall affects strips and kits distributed in the US and internationally.
Product
TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with TRUEresult and TRUE2go meters. TRUEread Blood Glucose Test Strips are available in vials with 10 ct., 25 ct., 50 ct., and sold as 10 ct. with meters. Quantitatively measure whole blood glucose in a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2886-2016·2016-10-05
Spacelabs Xhibit Telemetry Receiver Recall for System Lockups
Spacelabs Healthcare is recalling Xhibit Telemetry Receivers because the system may go offline or lock up, potentially failing to display alarms.
Product
Spacelabs Healthcare Xhibit Telemetry Receiver (XTR), Model 96280. Xhibit Telemetry Receivers (XTR) must be connected to an Xhibit Central Station for the display of patient vital signs.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2877-2016·2016-10-05
Siemens PRIMUS Linear Accelerators Recalled for Software Safety Issues
Siemens Medical Solutions is recalling 103 PRIMUS linear accelerators to install a software patch addressing several safety issues.
Product
PRIMUS, Accelerator, Linear, Medical The PRIMUSTM family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2895-2016·2016-10-05
Zyno Medical Administration Set Recalled for Potential Filter Leaking
Zyno Medical LLC is recalling 78,063 sterile administration sets due to a potential filter leaking defect. The sets are distributed nationwide for use with infusion pumps or gravity feed.
Product
Zyno Medical Administration Set, Sterile. RX For Use with Zyno Medical Infusion Pumps or Gravity Feed Product Code: B2-70071-DF Product Code: B2-70071-DF-120 (expanded recall) Product Usage: Zyno Medical Administration Set is a device used to administer fluids from a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2604-2016·2016-10-05
Dean Foods Recalls Meadow Gold Heavy Whipping Cream Due to Pasteurization Issues
Dean Foods is recalling specific containers of Meadow Gold Heavy Whipping Cream because they were not pasteurized sufficiently. Consumers in Idaho, Oregon, Wyoming, and Utah should check their products.
Product
Meadow Gold Dairy Pure Fresh Heavy Whipping Cream One Gallon (3.78L) in plastic one gallon container; Fresh Meadow Gold Dairy Pure Heavy Whipping Cream Half Pint (236 mL) in waxed cardboard carton; Meadow Gold Dairy Pure Fresh Heavy Whipping Cream One Quart (946mL) in waxed…
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-2888-2016·2016-10-05
Spiegelberg Brain Pressure Monitoring Probes Recalled for Measurement Errors
Spiegelberg is recalling 22 Brain Pressure Monitoring System probes due to air chamber shrinkage that caused false high readings in the lower measuring range.
Product
Spiegelberg Brain Pressure Monitoring System Probe 3PN, REF: SNDI3.1.531FV534P and Probe 3PS, REF: SNDI3.1.63/FV535P Product Usage: lntracranial pressure measuring probes are used to measure intracranial pressure (intracranial pressure, ICP), so the pressure in the head.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2881-2016·2016-10-05
Trividia Health Recalls TRUEread Blood Glucose Test Strips for Inaccurate Readings
Trividia Health is recalling TRUEread Blood Glucose Test Strips because they may provide incorrect low blood glucose levels.
Product
TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with TRUEresult and TRUE2go meters. TRUEread Blood Glucose Test Strips are available in vials with 10 ct., 25 ct., 50 ct., and sold as 10 ct. with meters. Quantitatively measure whole blood glucose in a…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V710000·2016-10-05
Altec Recalls 2014-2015 Aerial Devices Due to Boom Tip Cover Defect
Altec is recalling 219 model year 2014-2015 aerial devices because an improperly sized boom tip cover opening may allow contact with energized conductors, increasing injury risk.
Product
ALTEC — ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2893-2016·2016-10-05
Zyno Medical Administration Set Recalled for Potential Filter Leaking
Zyno Medical LLC is recalling 114,081 sterile administration sets due to a potential filter leaking defect. The sets are used to administer fluids to patients' vascular systems.
Product
Zyno Medical Administration Set, Sterile. Rx For Use with Zyno Medical Infusion Pumps or Gravity Feed Product Code: A2-80071-DF Product Code: A2-80071-DF-120 (Expanded recall) Product Usage: Zyno Medical Administration Set is a device used to administer fluids from a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2885-2016·2016-10-05
Spacelabs Xhibit Central Station Recalled for System Lockups and Alarm Failures
Spacelabs Healthcare is recalling Xhibit Central Stations because the telemetry system may go offline, lock up, or fail to display audio and visual alarms for asystole.
Product
Spacelabs Healthcare Xhibit Central Station, Model 96102, Version 1.1.2. Xhibit Telemetry Receivers (XTR) must be connected to an Xhibit Central Station for the display of patient vital signs.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V711000·2016-10-05
Western Star Trucks Recall for Seat Belt Mounting Plate Defect
Daimler Trucks North America is recalling 2014-2017 Western Star 4900 and 5700 trucks because a seat belt mounting plate may have a hole that is too large, increasing injury risk in a crash.
Product
WESTERN STAR — WESTERN STAR 5700, 4900
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2894-2016·2016-10-05
Zyno Medical Administration Set Recalled for Potential Filter Leaking
Zyno Medical LLC is recalling 78,069 sterile administration sets because the filter may leak. The sets are used to administer fluids to patients.
Product
Zyno Medical Administration Set, Sterile. Rx For Use with Zyno Medical Infusion Pumps or Gravity Feed Product Code: A2-80072-F Product Usage: Zyno Medical Administration Set is a device used to administer fluids from a container to a patients vascular system through a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2878-2016·2016-10-05
Siemens Syngo RT Therapist Software Recalled for Safety Issues
Siemens Medical Solutions is recalling Syngo RT Therapist software to address several safety issues. The recall affects 103 linear accelerators nationwide.
Product
Syngo RT Therapist, Accelerator, Linear, Medical Syngo RT Therapist is a software application whose indication for use includes the viewing, processing, filming, and archiving of medical images. It also permits patient data management, patient selection/setup, patient…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2876-2016·2016-10-05
Siemens ARTISTE Linear Accelerators Recalled for Software Safety Issues
Siemens Medical Solutions is recalling 103 ARTISTE linear accelerators to install a software patch addressing several safety issues.
Product
ARTISTE, Accelerator, Linear, Medical The intended use of the SIEMENS branded ARTISTETM family of linear accelerator systems is to deliver X-Ray photon and electron radiation for the therapeutic treatment of cancer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2879-2016·2016-10-05
CareFusion Recalls Alaris Syringe Modules Due to Software Anomaly
CareFusion 303, Inc. is recalling Alaris Syringe Module Model 8110 units with software version 9.15 because a software anomaly may cause infusions to stop unexpectedly.
Product
Alaris Syringe Module Model 8110 with software version 9.15 The Alaris Syringe Pump module is part of the Alaris System. The syringe pump delivers fluids in a manner similar to current syringe pumps on the market. Up to four Alaris Syringe pump modules can be connected to the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2892-2016·2016-10-05
Siemens Medical Solutions Recalls Syngo.plaza VB10A Picture Archiving Systems
Siemens Medical Solutions USA, Inc. is recalling 47 Syngo.plaza VB10A Picture Archiving and Communication Systems to eliminate several software issues.
Product
Syngo.plaza VB10A, Picture Archiving and Communication System
Category
Medical Device
Distribution
Distributed nationwide