Colorado recalls

Medline has recalled specific lots of its Nail Kit (Model DYKM1528) because the sterile saline wound wash included in the kit may not meet required sterility standards. The saline solution could potentially be contaminated. No injuries have been reported so far.

Medline recalled five models of Convenience Kits because the sterile saline wound wash component may not meet required sterility safety standards. The affected kits were distributed for medical use. No injuries have been reported.

Medline is recalling specific lots of its Convenience Nail Kit because the sterile saline wound wash component may not meet required sterility standards. The affected product was distributed nationwide and to several Caribbean locations. No injuries have been reported.

Medline Industries recalled its 7.1 FL OZ Sterile Saline Wound Wash because the manufacturer may not have properly sterilized the product to meet safety standards. This affects all lots of model MDSALINE7 distributed nationwide and in the Caribbean. No injuries have been reported.

Potential contamination with Salmonella.

Koi Koi Trading's frozen fish balls (4-piece packs, 5 lbs) contain wheat and sesame that are not listed on the label. These are serious allergens that can cause severe reactions in people with allergies. The affected product has item number 27530 and expiration date of 11/11/2027.

Koi Koi Trading's frozen fish balls (20 pieces, 400g) contain wheat and sesame that are not listed on the label. These are major food allergens that can cause serious allergic reactions in people with sensitivities. The product was distributed to restaurants and grocery stores across eight states.

Koi Koi Trading's frozen fish balls (40-piece, 200g packs, UPC 810093891338) contain wheat and sesame that are not listed on the label. This poses a serious risk to people with wheat or sesame allergies. The affected product was distributed to restaurants and stores across multiple states.

Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft paper/plastic bag pieces.

BioGlo Fluorescein Sodium Ophthalmic Strips were not manufactured according to safety standards, raising concerns about sterility. The strips are used by eye care professionals for diagnostic eye exams. All lots distributed nationwide are affected.

Bio Glo Fluorescein Sodium Ophthalmic Strips USP were not manufactured following proper sterility standards. These diagnostic strips, distributed nationwide, may not be sterile and could pose a safety risk if used in the eye.

Wizcure Fluorescein Sodium Ophthalmic Strips (1mg) were not manufactured following proper sterilization standards. These strips are used by eye care professionals to examine the eye surface. Because sterility cannot be assured, there is a potential risk of contamination.

Vista Gonio Eye Lubricant (hypromellose ophthalmic solution) distributed by hi-health was not manufactured following required safety standards, raising concerns about sterility. All lots of this eye drop product are affected. No injuries have been reported to date.

Vista Meibo Tears Propylene Glycol 0.6% eye drops were not manufactured under proper safety conditions, raising concerns about sterility. The FDA issued a recall of all lots distributed nationwide. No injuries have been reported.

Vista Gel Hypromellose eye drops were not manufactured according to FDA safety standards, which means the product may not be sterile. The eye drops were distributed nationwide in the United States. No injuries have been reported.

Vista Tears eye drops were manufactured without proper sterility controls, which means they may not be safe for use in the eye. No injuries have been reported, but the product does not meet FDA safety standards.

Agebox iKids-Growth Night Formula contains ibutamoren, a substance not listed on the label or approved by the FDA for this product. The affected 60-count bottles were sold online through Agebox.com and Amazon.com. No injuries have been reported.

Agebox iKids-Growth Day Formula capsules contain an undeclared drug ingredient called ibutamoren that was not approved by the FDA. The product was sold without proper FDA authorization. This affects 60-count bottles with lot numbers 23101201, 24080801, and 25020701.

Slate Run Pharmaceuticals is recalling Eptifibatide Injection 75 mg/100 mL vials because the carton label says "weight-adjusted bolus dosing" when it should say "weight-adjusted infusion." This labeling error could lead to incorrect administration of the medication. No injuries have been reported.

AvKARE is recalling one lot of Amantadine HCl 100 mg capsules because they failed to meet dissolution specifications—meaning the capsules may not break down properly in the body, affecting how much medicine you receive. This is a quality issue identified during manufacturing testing. No injuries have been reported.

LEO Pharma is recalling specific lots of Adbry, a prescription injection used to treat atopic dermatitis, because one unit was found to contain wool fiber particles. This contamination raises concerns about sterility and safety. No injuries have been reported so far.

Ajinomoto Foods North America is recalling frozen fried rice, ramen, and shu mai (dumpling) products sold under Ajinomoto, Kroger, Ling Ling, Tai Pei, and Trader Joe's brand names due to possible glass fragments in the food. The glass came from carrots used in the products. No injuries have been reported so far.

Several beef jerky products sold in Hawaii and online contain soy lecithin that is not listed on the label. Soy is a common allergen that can cause serious reactions in people with soy allergies. The products are no longer being sold, but some may still be in home pantries.

Evajoy above-ground pools 48 inches tall or larger have a compression strap around the outside legs that can act as a foothold, allowing children to climb into the pool. This creates a drowning risk even if the ladder is removed.

The display unit (parent unit) of Babysense Max View Baby Monitors can overheat or spark while charging, creating a fire risk. The affected model is VBM55, sold online from January 2023 through December 2025. Hisense has received 11 reports of overheating or sparking, but no injuries so far.

Andersen Windows is recalling opening control devices on 100 Series casement windows manufactured before November 19, 2025. These devices can break or detach after impact, allowing windows to open unexpectedly and creating a fall risk, especially for children. No injuries have been reported, but eight instances of device failure have been documented.

SumDirect LED mini lights contain small button cell batteries that children can easily remove and swallow, causing serious internal injuries or death. The product lacks required safety warnings and does not meet federal battery safety standards. About 1,600 units were sold online since 2016.

Todson's Concord 360 Degree Rechargeable Light-Up bike helmets (size large, black with LED lights) do not meet federal safety standards for retention and fit. The helmets may fail to stay in place or protect your head during a crash, creating a serious injury risk.

Joyreal busy board toys sold on Amazon have a small mirror that can detach, creating a choking hazard for children. The mirror also has sharp edges that can cause cuts. About 210 units were sold between September and November 2025.

Zelbuck children's chess games contain loose magnets that can come out and be swallowed by children. When high-powered magnets are ingested, they can stick together inside the stomach or intestines, causing serious blockages, tears, or life-threatening infections.