Kansas recalls

Liuqibax adult portable bed rails (Model BR-11) do not meet safety standards and can trap users between the rail and mattress, creating a risk of serious injury or death by asphyxiation. The rails also lack required hazard warning labels. About 12,000 units were sold on Amazon between July 2024 and May 2026.

These colorful silicone fidget sliders contain loose high-powered magnets that can be removed and swallowed. When multiple magnets are ingested, they can attract each other inside the digestive system, causing serious injury including intestinal perforation, blockage, and blood poisoning. A child has already been hospitalized after ingesting magnets from one of these sliders.

These infant walkers can pass through standard doorways and fail to stop at stairs, creating a fall hazard. They also have leg openings that allow children to slip down until their head becomes trapped. The walkers violate mandatory safety standards for infant walkers.

BUSOHA magnetic fidget sliders contain loose magnets that can be easily removed from the silicone casing. If swallowed by a child, these high-powered magnets can attract each other or metal objects in the digestive system, causing serious injury or death through intestinal perforation, twisting, or blockage.

These wooden dressers can tip over and trap children if not anchored to a wall. One child was injured in a tip-over incident. The dressers don't meet federal safety standards for furniture stability.

The bolts on Louisville Ladder brand attic stairway ladders can break while in use, creating a fall hazard. The company has received 11 reports of bolts breaking, including one injury. This affects over 1.7 million ladders sold since 2012.

The blades on certain DR Power PRO MAX30 walk-behind lawn mowers can keep running even after you release the control lever, or may start spinning without the control being engaged. This creates a serious risk of cuts or lacerations. The manufacturer has received 19 reports of this problem but no injuries yet.

Victory Medical Center Pharmacy identified elevated bacterial endotoxin levels in certain lots of its compounded glutathione 200 mg/mL multi-dose vials used for injection. Endotoxin contamination can cause serious reactions including fever, low blood pressure, severe headache, and in rare cases, anaphylactic shock or death. The pharmacy has received reports of adverse events from patients who received the product.

Medline Industries recalled Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits because the electrical connector at the Neptune humidifier can overheat, causing discoloration, melting, smoke, or burning. When this happens, the device automatically shuts off the heated wire function, which means infants may receive unheated or unconditioned breathing gas that can damage the airway and increase the risk of respiratory complications.

Fresenius Kabi recalled one lot of Morphine Sulfate Injection 2 mg/1 mL prefilled syringes due to a labeling error. Packages labeled as morphine may actually contain Dilaudid (hydromorphone), a different and more potent opioid. Using the wrong medication could cause serious respiratory problems or death, especially in patients not used to opioids or those with lung disease.

Boticelli Foods is recalling one lot of Bettergoods Pistachio Nut Butter (6.7 oz, UPC 194346207961, Lot LB028ACP04) distributed to Walmart stores in 19 states because it may be contaminated with Salmonella. No illnesses have been reported yet.

Liebel-Flarsheim Company is recalling one lot of OPTIRAY Imaging Bulk Package 350 (a radiographic contrast agent used in hospitals and imaging centers) because it contains particulate matter including plastic, stainless steel, and glass fragments. No adverse events have been reported so far, but contaminated product could cause local irritation, swelling, or in serious cases, blood vessel blockage or clots.

American Regent, Inc. Animal Health recalled four specific lots of Adequan Canine Injection (for dogs) and Adequan i.m. Injection (for horses) after discovering glass fibers in the products during internal testing. No adverse events have been reported to date.

BD is recalling specific lots of its Intraosseous Vascular Access System Needle Sets because some users have had difficulty removing the obturator (stylet) after needle placement. The affected needle sets were manufactured with out-of-tolerance dimensions and distributed between September 2024 and June 2026. If the obturator cannot be removed, clinicians may need to obtain alternative vascular access, potentially delaying urgent care.

Woodure tower step stools can collapse or tip over during use. Children's torsos can fit through openings on the front and back, creating a risk of entrapment, falls, and serious injury. The company has received 22 reports of tip-overs, including 15 injuries.

This baby doll playset includes small accessories like a pacifier, spoon, toothbrush, and soap dish that can be swallowed by young children. The toy is marketed for children under three years old but contains parts small enough to choke on, violating federal safety rules.

Mangohood Direct kids kitchen tower stools (model LT003) can collapse or tip over during use. The openings on the front and back are large enough for a child's torso to fit through, creating a serious risk of entrapment, falls, and injury.

Jake's Fireworks World Class Fireworks "Skull Strobe" rockets can explode before reaching their intended height, creating serious explosion and burn hazards. The wooden-stick rockets were sold at fireworks retailers nationwide between March 2025 and June 2026. No injuries have been reported.

The electrical cord on OCTROT heated throws and blankets can detach and ignite, creating a fire hazard. The company has received reports of 27 fires and 15 burn or electrical shock injuries linked to the product.

HARPPA's Nordi toddler tower stools can collapse or tip over during use. The stools have openings on the front and back that are large enough for a child's torso to fit through, creating a risk of entrapment. The company has received three reports of stools collapsing or tipping, resulting in injuries including scrapes, cuts, and bruises.

Golden Link sold Fantastic Four drinking cups and Captain America popcorn helmet containers with LED lights at movie theaters. The products contain easily accessible button cell batteries that children can swallow, which can cause serious internal burns or death. The products also lack required warning labels.

Galanz retro-style refrigerators sold from 2019 to 2022 can develop electrical short circuits that ignite, creating a fire and burn risk. The company has received 34 reports of fires, including one that resulted in a death.

The rechargeable lithium-ion battery in BenQ GV31 portable projectors can overheat, creating a risk of fire and burns. BenQ has received three reports of overheating, including one case of hand burns. About 1,249 projectors are affected in the U.S.

KAIFAM 5-drawer dressers can tip over and trap children if not anchored to the wall. The dressers do not meet federal safety standards for furniture stability. About 1,980 units were sold online.

EnHomee 15-Drawer Dressers sold on Amazon can tip over and trap children if they are not anchored to the wall. The dressers do not meet federal safety standards for clothing storage units. About 12,800 units were sold between August 2024 and April 2026.

Trsmima backyard zipline kits sold on Amazon can fail during use in dangerous ways: the steel cable, seat, or turnbuckle can detach or break, causing falls; and the spring brakes don't slow riders safely, leading to collisions with trees or falls. At least 21 people have been injured, including fractures and concussions.

Karl Storz Flexible Hystero-Fiberscope Kits with certain serial numbers contain expired single-use endoscopic seals that may not maintain sterility during gynecological procedures. The affected seals expired in January 2023 and were distributed across 15 U.S. states.

The SafeOp Patient Interface (REF: AIX11240), part of the SafeOp 3 Neural Informatix System used during spine surgery, can lose or drop its nerve monitoring signal due to a software problem. When this happens, the device may show system errors, lose connection to the surgeon's tablet, and require a restart—potentially extending surgery time or changing the surgical plan.

Medline Industries is recalling nine types of surgical convenience kits that contain BD PurPrep solution. The solution may be contaminated with low levels of Bacillus species, a bacterium that could pose a risk if the kits are used in sterile procedures. The recall affects specific lot numbers of joint, spine, and neurological surgery kits distributed to hospitals and surgical centers in ten U.S. states.

Medline Industries recalled specific NEURO PACK medical convenience kits because the included BD PurPrep 26 mL solution may contain low levels of Bacillus species bacteria. The contamination was identified in kits distributed to hospitals and medical facilities in 10 U.S. states.