Utah recalls
3,539 federal recalls affecting Utah in the last 12 months - 190 Utah-specific plus 3,349 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-09-09FDA-DrugGolden State Medical SupplyNot Yet ClassifiedNationwideGolden State Medical Supply Prasugrel tablets recalled for dissolution failure
Golden State Medical Supply Inc. is recalling Prasugrel HCI 10mg tablets (lot GS062298, expiration 09/30/2026) because they failed to meet dissolution specifications during quality testing. Dissolution is how quickly a tablet breaks down in the body to release its active ingredient. Tablets that dissolve too slowly or incompletely may not work as intended.
- 2026-09-09FDA-FoodLexunderClass IFood to Live SuperGrass Powder recalled for Salmonella
Food to Live Organic SuperGrass Powder in 6 oz, 12 oz, 1 lb, and 4 lb containers has been recalled due to Salmonella contamination. The affected products were distributed across the United States and U.S. Virgin Islands. No illnesses have been reported.
- 2026-09-09USDADe ToditoClass IDe Todito snack mix recalled for import violation
El Eden Import Distributor Corp. recalled pork cracklings snack products imported from Colombia, which is not approved to export meat products to the U.S. The products were shipped to distributors and retail locations in New Jersey and Utah in July 2026. No illnesses have been reported.
- 2026-09-07FDA-PRBMC MedicalNationwideBMC Luna G3 APAP recalled for firmware defect
BMC Medical Co., Ltd. recalled 20,160 Luna G3 APAP sleep apnea devices (Model LG3600) due to a firmware defect in version G3-2.00.76. Under certain high-pressure, high-breathing-rate conditions, affected devices can display an error message and shut down automatically, stopping therapy delivery. Most devices were corrected with a firmware upgrade, but up to 196 units may still contain the defective version.
- 2026-09-04FDA-PRFoods AliveNationwideFoods Alive moringa leaf powder recalled for Salmonella risk
Foods Alive Inc is recalling 8-ounce packages of organic moringa leaf powder because they may be contaminated with Salmonella. The contamination was discovered after the supplier's sample tested positive. No illnesses have been reported so far.
- 2026-09-03FDA-PRSupplx.comNationwideSUPPLX.com supplements recalled for undeclared yohimbine
SUPPLX.com's Business Pill and Branch Manager for Men dietary supplements contain yohimbine that is not listed on the labels. FDA testing found dangerously high levels of this substance, which can cause serious heart problems, severe high blood pressure, and other dangerous side effects—especially in people taking stimulants or certain medications.
- 2026-09-03FDA-PRAmerican RegentNationwideAmerican Regent epinephrine injection recalled for particulate contamination
American Regent is recalling three lots of epinephrine injection (1 mg/mL multi-dose vials) due to leaking and cracked vials, plus contamination with particles including nylon, cellulosic, acrylic, polyethylene, and glass. These particles can block blood vessels, cause blood clots, and damage organs; cracked vials also risk loss of sterility and bacterial contamination. No adverse events have been reported so far.
- 2026-09-03CPSCMondrakerNationwideMondraker bicycles recalled for handlebar fracture risk
Certain Mondraker mountain bicycles equipped with ONOFF S9 Carbon MTB handlebars may have handlebars that crack or fracture during use. This can cause loss of control and a fall. The company has received five reports of handlebar breakage, including two injuries from falls.
- 2026-09-03CPSCCloroxNationwideMistolin and Lestoil cleaners recalled for bacterial contamination
Clorox Puerto Rico is recalling about 6.3 million bottles of scented Mistolin and Lestoil cleaners sold in Puerto Rico and the U.S. Virgin Islands. The products may contain Pseudomonas aeruginosa bacteria, which can cause serious infections in people with weakened immune systems or external medical devices if the bacteria is inhaled, touches the eyes, or enters through a break in the skin. People with healthy immune systems are typically unaffected.
- 2026-09-03CPSCTruststoneNationwideXO Poppy Power Trip power banks recalled for fire risk
The lithium-ion battery in XO Poppy Power Trip Magnetic Wireless Power Banks (model PYPBK5M) can overheat and catch fire. About 32,400 units were sold at TJX and Marshalls stores in three colors: cream, cream with pink bow print, and black with teddy bear print. No injuries have been reported.
- 2026-09-03CPSCSkip HopNationwideSkip Hop Elmo teether recalled for choking hazard
The black eyes on this teether can detach when frozen, creating a choking risk for babies. Skip Hop has received four reports of eyes coming off, though no injuries have been reported yet.
- 2026-09-03CPSCGIHNJSINationwideGIHNJSI Squeezy Dumplings toys recalled for choking hazard
These squishy toys contain water beads that can expand if swallowed, potentially causing choking, intestinal blockage, and serious injury or death. The toys are translucent squishy balls with cartoon faces, sold in tan bamboo steamer-shaped containers.
- 2026-09-03CPSCOKK TradingNationwideOKK Trading squishy bun toys recalled for water bead ingestion risk
OKK Trading's Rainbow Mystery Squishy Bun Toys contain water beads that can expand larger than safe limits. If a child swallows a water bead, it can cause choking, intestinal blockage, and serious injury or death.
- 2026-09-03CPSCGizoon DirectNationwideGizoon Direct dressers recalled for tip-over hazard
Gizoon Direct six-drawer dressers can tip over if not anchored to the wall, creating a risk of serious injury or death to children. The dressers do not meet federal safety standards for furniture stability.
- 2026-09-03CPSCBranchNationwideBranch ergonomic chairs recalled for backrest detachment risk
The backrests on certain Branch height-adjustable ergonomic chairs can detach due to incorrectly installed anchors at the factory. This poses a fall hazard. The chairs were made between September 10, 2025 and April 22, 2026. Branch has received 11 reports of backrest detachment but no injuries so far.
- 2026-09-03CPSCDaikinNationwideAmana air conditioners recalled for fire hazard risk
Certain Amana brand through-the-wall air conditioners and heat pumps can develop a short circuit in the snubber component, which may emit flames. Two incidents of this short circuit have been reported, though no injuries have occurred yet.
- 2026-09-03CPSCLoyodaNationwideLoyoda adult portable bed rails recalled for entrapment risk
Loyoda adult portable bed rails do not meet federal safety standards for adult bed rails. They pose a risk of serious injury or death from entrapment and asphyxiation.
- 2026-09-03CPSCSheinNationwideSHEIN spiral toys recalled for choking hazard
SHEIN Distribution Corporation is recalling spiral toys that contain small plastic balls. These toys are intended for children under three years old, but the small balls pose a serious choking hazard and violate federal safety rules for that age group.
- 2026-09-03CPSCAudio PartnershipNationwideCambridge Audio Yoyo (M) speakers recalled for fire hazard
The lithium-ion batteries in Cambridge Audio Yoyo (M) Portable Bluetooth Speakers can overheat and catch fire. The company has received four reports of fires, smoke, and battery material ejection, though no injuries have been reported so far.
- 2026-09-03CPSCWu HaiNationwideAlanca 6-Drawer Dressers recalled for tip-over risk
These wooden dressers can tip over and trap children if not securely anchored to the wall. The dressers do not meet federal safety standards for clothing storage furniture. No injuries have been reported.
- 2026-08-29FDA-PRNorthwest NaturalsNationwideNorthwest Naturals pet food recalled for Salmonella, Listeria risk
Northwest Naturals has recalled two frozen raw pet food products because they may be contaminated with Salmonella and/or Listeria monocytogenes. The affected products are the Frozen Chicken Recipe (cat food, 2 lb. bags) and Frozen Raw Diet for Dogs Chicken Recipe (6 lb. bags) in specific lots. No illnesses have been reported so far.
- 2026-08-28FDA-PREverything SproutsNationwideEverything Sprouts radish mix recalled for E. coli and Salmonella risk
Everything Sprouts, LLC is recalling certain lots of Robust Radish Sprout Mix (5oz cups) sold in Minnesota and Wisconsin from August 13–26, 2026, because they may contain Shiga toxin-producing E. coli (STEC) or Salmonella bacteria. No illnesses have been reported to date.
- 2026-08-27FDA-PRB. BraunNationwideB. Braun saline injection recalled for particulate contamination
B. Braun Medical Inc. is recalling three lots of 0.9% Sodium Chloride Injection (saline solution) used in hospitals and healthcare settings. The recalled product contains particles of zinc oxide that should not be present. Intravenous fluids contaminated with particulate matter can cause serious complications including blood clots and organ damage. No injuries have been reported so far.
- 2026-08-27FDA-PRLipofitNationwideLipofit Extreme Fat Burner recalled for hidden prescription drug and toxic substance
Lipofit Extreme Fat Burner 2.0 (Lot 25M12F, expiration 09/2027) contains undeclared fluoxetine, a prescription antidepressant, in the daytime tablets and undeclared 2,4-dinitrophenol (DNP), a toxic pesticide, in the nighttime tablets. Neither ingredient is approved for use in dietary supplements, and DNP is not approved by the FDA for any use in humans.
- 2026-08-26FDA-PRRevival Animal HealthNationwideBreeder's Edge and Shelter's Choice kitten milk recalled for nutrient deficiency
Revival Animal Health recalled Breeder's Edge® and Shelter's Choice® Feline Milk Replacers because some batches contain low levels of potassium, copper, folic acid, choline, and/or vitamin B6. Young kittens depend entirely on milk replacer for nutrition, and these deficiencies can cause anemia, organ damage, and developmental problems within days or weeks.
- 2026-08-26FDA-PRBaxterNationwideBaxter sodium citrate solution recalled for fiberglass contamination
Baxter is recalling one lot of Anticoagulant Sodium Citrate Solution used with apheresis devices due to potential fiberglass particles in the solution. The affected product was distributed to one customer in the United States between July 2 and July 11, 2026. No adverse events have been reported to date.
- 2026-08-25FDA-PRDonutfulNationwideDonutful cake donuts recalled for undeclared milk allergen
The Better Bakehouse Snack Company recalled certain lots of Donutful Chocolate Dipped Vanilla Cake Donuts because they may contain milk that is not listed on the label. People with a milk allergy or severe sensitivity could have a serious allergic reaction if they eat this product.
- 2026-08-25FDA-PRBaxterNationwideBaxter saline injection recalled for fiberglass contamination
Baxter is recalling two lots of 0.9% Sodium Chloride Injection (saline solution) used in hospitals and dialysis centers because fiberglass particles have been found in the solution. The affected lots were distributed to hospitals and medical suppliers in 14 states between July 31 and August 3, 2026. No injuries have been reported so far.
- 2026-08-25FDA-PRBaxterNationwideBaxter dextrose injection recalled for stainless steel particles
Baxter is recalling one lot of 70% Dextrose Injection used in hospitals and care facilities because stainless steel particles were found in the solution. If given intravenously, these particles could cause blood clots, block blood vessels, or damage organs. No patient injuries have been reported so far.
- 2026-08-21FDA-PRVitruvias TherapeuticsNationwideVitruvias Thyroid Tablets recalled for super potency risk
Vitruvias Therapeutics is recalling one lot (504950) of Thyroid Tablets, USP 30 mg because testing found the tablets may contain higher-than-intended amounts of thyroid hormone. Taking overly potent thyroid medication can cause an overactive thyroid, leading to weight loss, rapid heartbeat, chest pain, and other serious symptoms, especially in elderly people, pregnant women, and infants.
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