Vermont recalls

Fresenius Kabi USA is recalling specific batches of 0.9% Sodium Chloride Injection (saline) because the manufacturer cannot confirm the product is sterile. Sterility is critical for injectable medications. The affected batches have expiration dates of October 31, 2026, or November 30, 2026.

Fresenius Kabi is recalling specific batches of 0.9% Sodium Chloride Injection due to a lack of assurance that the product is sterile. This injectable solution is used in medical settings and could pose a risk if contaminated. No injuries have been reported to date.

Fresenius Kabi USA is recalling multiple batches of 0.9% Sodium Chloride Injection (saline solution) used for medical purposes because the manufacturer cannot guarantee the product is sterile. The affected batches were distributed nationwide, Alaska, and Puerto Rico. No injuries have been reported.

Fresenius Kabi is recalling specific batches of 0.9% Sodium Chloride Injection (saline) in 100 mL bags due to lack of assurance of sterility. The affected batches were distributed nationwide, including Alaska and Puerto Rico. No injuries have been reported.

Fresenius Kabi is recalling specific batches of 0.9% Sodium Chloride Injection because the manufacturer cannot guarantee these vials are sterile. This injectable medication is used in hospitals and clinical settings. No injuries have been reported.

Fresenius Kabi is recalling one batch of 0.45% sodium chloride injection (saline solution) used in hospitals and medical facilities because the manufacturer cannot guarantee the product is sterile. The affected batch is #6402413 with an expiration date of 02/29/2028. No infections or injuries have been reported so far.

Cipla USA is recalling specific lots of Lanreotide Injection (120 mg) because the manufacturer did not follow proper visual inspection procedures during production. This means the medication may not meet sterility standards and could potentially be contaminated.

Cipla USA is recalling specific lots of Lanreotide Injection 120 mg due to concerns about sterility. The FDA found deficiencies in the manufacturer's visual inspection procedures, which could mean some syringes may not be properly sterilized. No injuries have been reported so far.

Morovan gel nail polish remover (15ml bottle, turquoise with white cap) was found to contain methylene chloride and chloroform—chemicals prohibited in cosmetics. Methylene chloride may cause cancer and is not allowed in cosmetics at any level under FDA regulations. About 4,000 units were sold on Amazon between August 2025 and January 2026.

Muscccm-branded pool drain covers sold on Amazon do not meet federal safety standards for drain protection. These covers create a risk that swimmers could become trapped or drown. About 480 covers were sold between February and March 2026.

Prestige Import Group is recalling about 4,300 Supernova and Typhoon brand butane lighters because they lack the required child-resistant safety mechanism. These lighters do not meet federal safety standards and pose a risk of fire and burn injuries, especially to children. No injuries have been reported.

Happiness Light LED lights sold on Amazon contain easy-to-access coin batteries that children can swallow. Ingesting these batteries can cause serious internal burns and death. The lights also lack required safety warnings.

Shenzhen Shijingjie male-to-male extension cords (model RY-US-06 and RY_US-1.5) sold on Walmart.com have exposed live prongs that can cause electrocution. These cords are sometimes used to connect generators to home outlets during power outages, which can backfeed electricity into the home's wiring and create fire risk. Their short length also encourages generators to run near homes or indoors, risking carbon monoxide poisoning.

The lithium-ion battery in VEEKTOMX VT103 power banks can overheat and catch fire. The company has received three reports of fires causing minor property damage. The power banks were sold on Amazon between January and September 2024.

ShymeryDirect LED lights contain easily accessible lithium coin batteries (CR2032) that children can swallow, causing serious internal burns or death. The lights lack required safety warnings and violate federal battery safety standards.

Yeeluzan pool drain covers sold on Amazon do not meet federal safety standards and can trap swimmers underwater, creating a drowning risk. About 640 white plastic drain covers (8.7 inches diameter, sold in two-packs) were sold from May 2025 through March 2026.

Halloween pumpkin carving kits sold on Amazon contain tea light candles with button cell batteries that children can easily remove and swallow. Swallowing these batteries can cause serious internal injuries, chemical burns, and death. The kits lack required safety warnings.

Head USA ski boots from 2015–2022 with fluorescent yellow shells or soles can deteriorate and break during use, creating a serious fall risk. The company has identified specific model numbers and article codes affected by this defect. No injuries have been reported, but the boots pose a hazard if worn.

The wires in this decorative light-up buck can be connected incorrectly at the factory, causing a resistor to overheat. This creates a risk of burns or fire. The company has received five reports of smoke and burning smells.

The D-ring handle on SCUBAPRO Monorail Weight Pockets can detach during diving. If this happens, you won't be able to remove the weight pocket in an emergency to surface safely, creating a serious drowning risk. The company has received two reports of handles detaching, though no injuries have occurred yet.

Maitys magnetic drinkware charms sold on Amazon contain loose magnets that can separate and be swallowed by children. High-powered magnets in the digestive system can attract each other or metal objects, causing serious internal injuries including intestinal perforation, blockage, and potentially death.

Silks children's loungewear sets (sizes 2T–13/14) do not meet federal flammability standards for sleepwear and pose a burn hazard to children. The two-piece sets include a short-sleeved shirt with matching shorts or pants and were sold online from January 2024 through September 2025.

Snooz's Breez 2-in-1 Smart Bedroom fan can overheat and catch fire due to corrosion in the power connector. The company has received six reports of fans overheating and smoking, including one confirmed fire. No injuries have been reported so far.

Easymake adult 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. About 19,000 units were sold online starting in August 2023.

Vitaquest International is recalling multiple iron-containing dietary supplements sold under brands including Arey, Bari Life, Bird&Be, Biote, Dr. Fuhrman, NuLife, HMR, Bariatric Pal, Noevir, Zenbean, and Sakara. The packaging does not meet federal child-resistant requirements, creating a serious poisoning risk if young children swallow the contents.

BISSELL steam cleaner attachments can unexpectedly detach during use and spray hot water or steam, causing burn injuries. The company has received over 200 reports of attachments detaching, including 161 burn injuries. This affects over 1.7 million units sold between October 2024 and March 2026.

Wybotics robotic pool vacuums (Osprey 700 Max and S1 models) have lithium-ion batteries that can overheat and catch fire during charging or normal use. The company has received 10 reports of overheating or fires, with 9 cases of property damage but no injuries so far. Only specific serial numbers are affected.

Blaine Labs is recalling three lot numbers of Revitaderm and Tridergel wound care gel (1 oz. and 3 oz. bottles/tubes) because they may contain Lysinibacillus fusiformis, a bacterium found in the environment. The affected products were distributed to healthcare providers only, not sold in stores. No injuries have been reported so far.

Cardinal Health Monoject Tuberculin Syringes labeled as 1 mL Luer Lock (Catalog 1180100777) actually contain U-100 Insulin syringes inside the packages. This mislabeling could lead to incorrect dosing if the syringes are used without checking the actual contents. The affected lot numbers are 531164X and 531162X.

GE Healthcare SIGNA Premier whole-body MRI scanners may have steel fittings instead of brass fittings on the magnet rear. During service work while the magnet is powered up, the magnetic field could pull on these steel parts, risking injury to technicians.