Utah recalls
1481 federal recalls on file affecting Utah - 69 Utah-specific plus 1412 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-03-26CPSCSunnyyesNationwideStop using Sunnyyes LED mini lights immediately
The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because the lights contain lithium coin batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the screw used on the remote controls to secure the battery compartments that contain a lithium coin battery does not remain attached. Also, the packaging does not have the warnings as required by Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- 2026-03-26CPSCDuraTracNationwideStop using DuraTrac gas connectors
The recalled DuraTrac gas connectors contain a manufacturing defect that could cause a gas leak, posing a fire hazard to consumers.
- 2026-03-26CPSCAirClubNationwideStop using AirClub convertible bassinets immediately
The recalled convertible bassinets violate the mandatory standard for bedside sleepers because the mechanism used to attach the product to the adult bed creates an opening between the bedside sleeper and mattress, posing a deadly fall hazard to infants.
- 2026-03-26CPSCVive HealthNationwideStop using Vive Health bed rails immediately
When the recalled bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress. This poses a serious entrapment hazard and risk of death by asphyxiation.
- 2026-03-26CPSC4our KiddiesNationwideStop using 4our Kiddies furniture straps immediately
The recalled plastic tip restraint kits (also referred to as furniture straps) can break or degrade, posing tip-over and entrapment hazards that can result in serious injuries or death to children or elderly consumers interacting with furniture that is secured to the wall with the defective plastic tip restraints. This is a hidden defect because consumers who purchase and install this product may be under a false sense of security that their furniture is safe from a tip-over incident.
- 2026-03-26CPSCNexgrillNationwideStop using Nexgrill grill brushes immediately
Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that could require surgery.
- 2026-03-25FDA-DeviceDatascopeClass IIINationwideCheck your Datascope battery charger left bay
The Battery Charging Station is an optional dual-bay charger used to charge the Cardiosave IABP Lithium- Ion batteries when they are not being used to operate the IABP. Getinge has identified that a protruding screw in the left battery bay limits full insertion of certain batteries and prevents proper charging. The right bay of the Battery Charging Station is not affected by this issue.
- 2026-03-25FDA-DeviceHologicClass IINationwideStop using Hologic Aptima HPV Assay kits
Due to product exhibiting potential to generate either invalid or false negative results.
- 2026-03-25FDA-DeviceDiagnostica StagoClass IINationwideStop using STA Liatest D-Di test kits
After receiving customer complaints, investigations confirmed the presence of a positive bias in D-Dimer measurements throughout the entire analytical range.
- 2026-03-25FDA-DeviceConvaTecClass IINationwideStop using ConvaTec EsteemBody Drainable Pouch
Drainable large pouch may leak due to manufacturing issue.
- 2026-03-25FDA-DeviceConvaTecClass IINationwideStop using ConvaTec EsteemBody Drainable Pouch
Drainable large pouch may leak due to manufacturing issue.
- 2026-03-25FDA-DeviceConvaTecClass IINationwideStop using ConvaTec EsteemBody Drainable Pouch
Drainable large pouch may leak due to manufacturing issue.
- 2026-03-25FDA-DeviceElektaClass IINationwideCheck your Leksell Gamma Knife serial number
Due to adapter not being properly aligned or locked in place.
- 2026-03-25FDA-DeviceStrykerClass IINationwideCheck your Stryker Cub crib serial number
Cribs sold in the USA are missing two access door warning labels.
- 2026-03-25FDA-DeviceLeMaitre VascularClass IINationwideCheck LeMaitre Vascular Artegraft Graft packaging
Labeling mix-up resulting in the incorrect lot outer packaging of product.
- 2026-03-25FDA-DeviceBaxterClass IINationwideStop using Welch Allyn Vision Screener VS100
Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in susceptible individuals.
- 2026-03-25FDA-DeviceHowmedica OsteonicsClass IINationwideStop using Howmedica MICS3 Saw Attachment
A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which secure the cover to the Angled Saw Housing, may loosen during use and detach from the attachment.
- 2026-03-25FDA-DeviceGEClass IINationwideUpdate GE Centricity Universal Viewer software
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
- 2026-03-25FDA-DeviceGEClass IINationwideUpdate GE Centricity Universal Viewer software
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
- 2026-03-25FDA-DeviceGEClass IINationwideUpdate GE Centricity Universal Viewer software
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
- 2026-03-25FDA-DeviceAbbottClass IINationwideStop using Abbott ID NOW flu test kit
It was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use.
- 2026-03-25USDAPublic Health AlertNationwideDo not eat Blackwing Organic Meats beef or pork
Produced Without Benefit of Inspection
- 2026-03-25FDA-FoodSaputoClass IIReturn Great Value cottage cheese to Walmart
Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
- 2026-03-25FDA-FoodSaputo CheeseClass IIStop using Great Value cottage cheese
Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
- 2026-03-25FDA-FoodSaputoClass IIStop using Great Value cottage cheese
Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
- 2026-03-25FDA-FoodSaputoClass IICLOVER SONOMA SOUR CREAM NET WT 8OZ UPC 0 70852 61800 5 & 16OZ UPC 0 70852 61500 4 DISTRIBUTED BY: CLOVER-STORNETTA FARMS LLC PETALUMA, CA 94952
Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
- 2026-03-25FDA-FoodSaputoClass IIStop using Clover Sonoma cottage cheese
Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
- 2026-03-25FDA-FoodKradjianClass INationwideStop using MID EAST Jordanian Zaatar spice mix
Undeclared allergen ingredients (sesame and wheat) in Zaatar Spice mix.
- 2026-03-25FDA-FoodWinder LaboratoriesClass IIICheck Winder Laboratories multivitamin bottles
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
- 2026-03-25FDA-DrugApotexClass IINationwideStop using Apotex brimonidine/timolol eye drops
Lack of Assurance of Sterility
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