Hawaii recalls

Lone Star Dairy Products LLC is recalling spray dried milk powder products because Salmonella bacteria was found during testing of finished products. The recall affects specific lot codes of NFDM Low Heat, NFDM High Heat, and SMP Medium Heat products sold in 25 kg bags and 1 metric ton totes.

Some cartons of Amneal Magnesium Sulfate IV bags were mislabeled and contained Tranexamic Acid (a different medication) instead. This mix-up affects lot AH250162 with an expiration date of 8/31/2027. The error was discovered before the product reached patients.

Appco Pharma LLC is recalling specific lots of prazosin hydrochloride 5mg capsules because they contain higher-than-acceptable levels of a nitrosamine impurity (N-nitroso-prazosin). Nitrosamines are chemical contaminants that may increase health risks with long-term exposure. This is a manufacturing quality issue, not a safety defect in the drug itself.

Appco Pharma LLC is recalling specific lots of prazosin hydrochloride 2mg capsules because they contain higher-than-allowed levels of a nitrosamine impurity called N-nitroso-prazosin. Nitrosamines are chemicals that may increase cancer risk with long-term exposure. No injuries have been reported so far.

Appco Pharma LLC is recalling prazosin hydrochloride 1mg capsules (100-count bottles) because they may contain higher-than-acceptable levels of a nitrosamine impurity. This impurity was detected during manufacturing quality checks. The recall affects specific lot numbers distributed nationwide.

Multiple brands of artificial tears eye drops made by K.C. Pharmaceuticals have been recalled because the manufacturer cannot confirm the product is sterile. The affected drops are sold under store brands including Leader, Good Sense, Good Neighbor Pharmacy, TopCare, Best Choice, Kroger, Publix, and Quality Choice. No injuries have been reported.

K.C. Pharmaceuticals issued a recall of Rugby Lubricating Eye Drops and Walgreens Lubricant Eye Drops because the manufacturer cannot guarantee the products are sterile. Non-sterile eye drops can introduce bacteria or other microorganisms into the eye. The recall affects specific lots (SY24K01 and SY24K02) with expiration dates of 09/30/26.

K.C. Pharmaceuticals has recalled multiple brands of sterile redness relief eye drops because they may not meet sterility standards. The affected products were distributed nationwide under various store and pharmacy brand names. No injuries have been reported so far.

K.C. Pharmaceuticals issued a recall of sterile eye drops sold under multiple brand names (including Walgreens, Good Sense, Kroger, CVS, and others) because the manufacturer cannot confirm the products remain sterile. The affected bottles were distributed nationwide. No injuries have been reported.

K.C. Pharmaceuticals is recalling multiple brands of ultra lubricating eye drops sold nationwide because the manufacturer cannot guarantee the drops are sterile. The affected products were distributed under names including Leader, Harris Teeter, Foster & Thrive, Walgreens, CVS Health, Kroger, Publix, Meijer, Good Sense, Quality Choice, and Avenova. No injuries have been reported.

K.C. Pharmaceuticals is recalling Dry Eye Relief Eye Drops sold under multiple store brands including Geri Care, TopCare, Rite Aid, Leader, and others due to concerns that the product may not be sterile. The recall affects 15 mL bottles with specific lot numbers and expiration dates sold nationwide.

K.C. Pharmaceuticals' Advanced Relief eye drops in 0.5 fl oz bottles may not be sterile due to a manufacturing issue. The affected products were sold under multiple store brands at Walgreens, Kroger, CVS, and other retailers nationwide. No infections have been reported so far.

K.C. Pharmaceuticals has recalled multiple brands of sterile eye drops (including Best Choice, Quality Choice, Discount Drug Mart, Good Sense, Walgreens, CareOne, Equaline, TopCare, Meijer, and H.E.B.) because the manufacturer cannot guarantee the products are sterile. Non-sterile eye drops can introduce infection into the eye. The affected products were distributed nationwide and have lot number AC24E01 with expiration date 05/31/26.

Amneal Pharmaceuticals is recalling specific lots of tramadol 50 mg tablets because they contain higher-than-allowed levels of a chemical impurity called N-nitroso-desmethyl-tramadol (NDSRI). The impurity was discovered during stability testing of tablets nearing the end of their shelf life. No injuries have been reported.

Alembic Pharmaceuticals is recalling specific lots of Bromfenac Ophthalmic Solution 0.07% because the medication failed purity and degradation tests during stability testing at 20 months. The affected eye drops may contain higher-than-acceptable impurity levels, which could affect safety and effectiveness.

Nalpac is recalling DTF Sexual Chocolate because it contains sildenafil and tadalafil—prescription drug ingredients found in Viagra and Cialis—that were not listed on the label. These hidden ingredients can dangerously lower blood pressure, especially if you take nitrate medications like nitroglycerin.

Liquid Blenz Corp. is recalling all Good Brain Tonic beverages (16 oz and 32 oz bottles) due to a potential botulism risk. Botulism is a serious form of food poisoning. No illnesses have been reported yet, but the product was distributed nationwide.

The USDA retracted a public health alert issued on April 1, 2026, for Walmart Great Value Fully Cooked Dino Shaped Chicken Breast Nuggets with a "Best If Used By" date of February 10, 2027. The initial alert was based on a laboratory test that showed elevated trace levels of lead, but follow-up testing found no lead contamination in the product. The USDA determined the original test result was a false positive caused by contamination in the laboratory during analysis, not in the food itself.

Raw Farm has recalled specific batches of raw cheddar cheese products (blocks and shredded) due to a potential link to an E. coli O157:H7 outbreak. The recall includes multiple batch numbers and expiration dates listed on the Raw Farm website. No pathogens have been found in Raw Farm products tested so far.

The canopy beams on certain Samson International bed frames can collapse, especially when the bed is moved. The company has received five reports of the canopy collapsing and striking people, resulting in shoulder and head injuries.

Tuymec Minoxidil Hair Growth Spray bottles sold on Amazon do not have child-resistant caps, violating federal safety rules. Minoxidil is toxic if swallowed by young children and can cause serious injury or death.

Sam's Club is recalling Member's Mark Valentine-themed children's pajama sets because they don't meet mandatory flammability standards for sleepwear. This poses a risk of burn injuries. About 18,000 sets were sold online between December 2025 and January 2026.

HTRC and Haisito brand T400 battery chargers can overheat and ignite, causing fires or explosions. The company has received 33 reports of fires and explosions, including three reports of injuries from burns and smoke inhalation.

Sangohe portable bed rails (models 504E and 504Q) can trap users between the rail and mattress, creating a serious risk of injury or death by asphyxiation. The rails also lack required warning labels. About 36,500 units were sold online starting August 2023.

The metal cap on the handle screw of these sauté pans can detach and eject forcefully when the pan is heated. E Mishan has received at least 98 reports of the cap detaching, including one case where a consumer was bruised and burned.

TecFlox minoxidil topical solution bottles do not have child-resistant packaging as required by law. The liquid inside can cause serious injury or death if a young child swallows it. About 900 bottles were sold on Amazon in October 2025.

ELENKER portable bed rails can trap users between the rail and mattress, creating a serious risk of injury or death by asphyxiation. The rails also lack required warning labels. The recalled models are silver collapsible rails sold on Amazon since August 2023.

OCUN NA is recalling certain Condor HMS Triple Carabiners sold from February 2025 through February 2026. The carabiner's gate can fail to close automatically and may require manual closing, which could cause the carabiner to fail during climbing and lead to a fall.

These Christmas light-up party favors contain button cell batteries that children can easily access and swallow. Swallowed button batteries can cause serious internal burns and death. The rings were sold on Amazon between August and December 2025.

These Halloween light-up rings contain easily accessible button cell batteries that children can remove and swallow. Swallowed button batteries can cause serious internal burns and death within hours. About 800 units were sold on Amazon between June 2025 and January 2026.