Product Recalls in Utah

Product recalls affecting Utah — including food, drugs, consumer products, medical devices, and vehicles distributed to Utah. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,666 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,666 in last 12 months

Showing 541560 of 49,677 recalls

Medical DeviceDecember 8, 2025· Securitas Healthcare LLC

Recalled Item: Arial 900 MHz Call Station Recalled by Securitas Healthcare LLC Due to...

The Issue: Securitas Healthcare has become aware of a firmware issue in the Call...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2025· LimFlow, Inc.

Recalled Item: Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog...

The Issue: Incorrect expiration date

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2025· Meridian Bioscience Inc

Recalled Item: Revogene C. difficile Recalled by Meridian Bioscience Inc Due to The...

The Issue: The affected lots show a decline in performance over time, which may lead to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2025· Beaver-Visitec International, Inc.

Recalled Item: BVI Leos Laser and Endoscopy System. Model Number: OME6000U. Recalled by...

The Issue: Manufacturing deviation in which the ferrites specified for the USB cable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodDecember 4, 2025· AZ Gems, Inc.

Recalled Item: Jumbo RAW SHRIMP Recalled by AZ Gems, Inc. Due to elevated levels of...

The Issue: elevated levels of chloramphenicol in frozen shrimp

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 4, 2025· Lil Turtles LLC

Recalled Item: Grandma Belle's Tomato Basil Soup Recalled by Lil Turtles LLC Due to...

The Issue: Undeclared allergen - milk

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Inflation...

The Issue: Inflation device handle may detach from the syringe during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

Recalled Item: Allwell Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation device handle may detach from the syringe during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

Recalled Item: Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Numbers:...

The Issue: Inflation device handle may detach from the syringe during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Inflation...

The Issue: Inflation device handle may detach from the syringe during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Inflation...

The Issue: Inflation device handle may detach from the syringe during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Inflation...

The Issue: Inflation device handle may detach from the syringe during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

Recalled Item: Allwell Angioplasty Pack /B Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation device handle may detach from the syringe during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Intuitive Surgical, Inc.

Recalled Item: Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Recalled...

The Issue: Due to probe bags that may have a compromised or incomplete sterile pouch seal.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Mobius Imaging, LLC

Recalled Item: Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Recalled by...

The Issue: AIRO pendant replacement kits and upgrade do not possess the "Safe Hand...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Mobius Imaging, LLC

Recalled Item: Detachable 10in Pendant Upgrade component for the AIRO Computed Tomography...

The Issue: AIRO pendant replacement kits and upgrade do not possess the "Safe Hand...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Medtronic Inc

Recalled Item: Abre Venous Self-Expanding Stent System Recalled by Medtronic Inc Due to...

The Issue: Stents may be impacted by a Nitinol anomaly which causes a reduced stent...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodDecember 3, 2025· McCain Foods USA Inc

Recalled Item: Sysco Imperial Potato Tater Barrel Recalled by McCain Foods USA Inc Due to...

The Issue: Clear hard plastic fragments.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 3, 2025· McCain Foods USA Inc

Recalled Item: Ore-Ida Tater Tots shaped potatoes Recalled by McCain Foods USA Inc Due to...

The Issue: Clear hard plastic fragments.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia Ambition S. Product Code (REF): 782108. MR systems with Recalled by...

The Issue: The potential for stiffness value errors when viewing exported MR...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing