Wisconsin recalls

Topkay torch lighters sold on Amazon lack required child-resistant safety features, creating a risk of serious burns or fire. About 7,500 black two-packs labeled "Honest" were sold between September and October 2025.

Gagaku ice cream shop toy playsets sold on Amazon contain high-powered magnets that can loosen and detach. If a child swallows these magnets, they can attract each other or metal objects inside the digestive system, causing serious injury including intestinal perforation, blockage, blood poisoning, or death.

Yetonamr Pull String Teething Toys have silicone strings that are smaller than safety standards allow. These strings can lodge in a child's throat and cause serious choking, breathing problems, or death. CPSC has received 32 reports of choking incidents.

The power cord on certain Matrix Retail and Vision treadmills can become loose where it connects to the machine, creating a fire hazard. About 47,000 treadmills are affected, manufactured between June 2007 and January 2024. The company has received 27 reports of overheating at the connection, though no injuries have occurred yet.

Academy Sports + Outdoors is recalling Magellan Odyssey Rocker Chairs sold between September and October 2025 because the chair legs can break. This poses a risk of falls and injury. The chairs have a metal frame with mesh backrest and were sold in charcoal, navy, olive green, and teal colors.

Angry Orange Enzyme Stain Remover products may contain Pseudomonas aeruginosa bacteria, which can cause serious infections in people with weakened immune systems, lung conditions, or external medical devices. The bacteria can enter the body through inhalation, eyes, or breaks in the skin. People with healthy immune systems are typically not at risk.

Certain batches of syringes in ICU Medical's Portex Spinal Tray may have cracks in the syringe collar. This defect can prevent the syringe from working properly, cause repeated blood draws, or lead to blood leakage during arterial blood sampling or fluid delivery.

ICU Medical Inc. is recalling specific lots of Pulsator Arterial Blood Sampling Kits because some syringes have cracks in the collar. This crack can cause blood to leak during sampling, delays in blood draws, or the need to repeat the procedure.

Thoratec CentriMag blood pump components used in acute circulatory support and ECMO systems may not lock securely into the motor. If the pump fails to lock properly, the system may not generate an alarm, which could delay critical heart support or cause serious complications.

Medtronic has recalled certain Abre Venous Self-Expanding Stents due to a manufacturing issue with the stent material (Nitinol) that can cause the stent to be smaller than intended when deployed. This reduced size may result in the stent moving out of position after placement.

Intuitive Surgical is recalling certain da Vinci SP Access Port Kits because the sterile trays may develop cracks during storage or handling. A cracked tray could allow bacteria or other contaminants to enter, compromising the sterile field during surgery. No injuries have been reported.

Instrumentation Laboratory has recalled a coagulation test reagent (Part Number 0020006800, Lot N1136730) used to evaluate blood clotting and monitor heparin therapy due to potential microbial contamination. The affected lot expires 12/31/2025 and was distributed worldwide including multiple U.S. states and countries. No injuries have been reported to date.

ICU Medical identified a batch of defective speakers in some Plum Duo Infusion Pumps that may fail silently. If the speaker fails, the pump will not produce audible alarms, alerts, or sound feedback when you touch the screen. This could delay recognition of important pump notifications.

Hologic's ThinPrep CytoLyt Solution (a buffered cell wash used in laboratory testing) from lot number 5062EC has been found to contain fungal contamination. The affected product was distributed nationwide. No injuries have been reported.

The Catalyst+ patient positioning system used in stereotactic radiosurgery (a type of radiation therapy) has a software issue that may cause incorrect patient positioning. In some cases, the system may show a patient is correctly positioned when they are actually outside the safe treatment area, which could affect treatment accuracy.

Philips Azurion X-ray imaging systems running software versions R2.1.10 or R2.2.10 may experience six different software problems. These include unexpected system restarts, continuous restart loops, storage space issues, and positioning errors that could affect image quality or system availability.

Medline medical procedure kits containing Stryker's Strykeflow 2 Suction Irrigators may leak irrigation fluid into the handpiece and battery pack during use due to a 2024 design change. Some devices have leaked fluid or released vaporized saline that may resemble smoke.

Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and battery pack during use of the Strykeflow 2 Suction Irrigator. This design change has caused some devices to leak and/or emit vaporized saline (which can resemble smoke) during use.

Medline medical procedure kits containing Stryker's Strykeflow 2 Suction Irrigators are being recalled due to a 2024 design change. The change allows irrigation solution to leak into the handpiece and battery pack during use, and some devices have emitted vaporized saline that resembles smoke. No injuries have been reported.

Medline medical procedure convenience kits containing Stryker's Strykeflow 2 Suction Irrigators have a design flaw that allows irrigation solution to leak into the handpiece and battery pack during use. Some devices have leaked fluid or emitted vaporized saline that may resemble smoke during procedures.

Medline medical procedure kits containing Stryker Strykeflow 2 Suction Irrigators may leak or emit vaporized saline during surgery due to a 2024 design change. The irrigation solution can travel into the handpiece and battery pack, potentially causing device malfunction or creating a smoke-like vapor in the surgical field.

Medline medical procedure kits containing Stryker Strykeflow 2 Suction Irrigators have a design flaw that allows irrigation fluid to leak into the handpiece and battery pack during use. Some devices have leaked or released vaporized saline that may resemble smoke. This affects specific thoracic and cardiac robotic surgery kits distributed nationwide.

Diagnostica Stago is recalling lot 271288 of the Asserachrom HPIA test kit, which detects antibodies related to heparin-induced thrombocytopenia (HIT type II). The affected lot may have defective test wells that produce false negative results, meaning the test could fail to detect the condition when it is present.

Heraeus Medical's PALACOS MV pro bone cement systems (models 5150633 and 5150635) have experienced increased reports of ampoule breakage during use. When ampoules fail to break properly or incompletely, the cement cannot form correctly and cannot be used in surgery.

Heraeus Medical's PALACOS MV+G pro bone cement (models 5081290 and 5081291) may have ampoules that fail to break properly during mixing. When ampoules don't break as intended, the cement cannot form correctly and cannot be used during surgery.

Heraeus Medical is recalling PALACOS R+G pro bone cement (models 5081288 and 5081289) because the ampoules inside the mixing system may fail to break properly. When ampoules don't break as intended, the cement cannot be prepared correctly for use during surgery.

Heraeus Medical is recalling PALACOS R pro 40 and R pro 80 bone cement products because the ampoules (small sealed containers) inside the mixing systems may not break properly during use. When ampoules fail to break, the bone cement cannot be prepared correctly and cannot be used during surgery.

Philips Medical Systems has recalled Azurion Systems R3.0 due to nine software issues that may cause X-ray loss, system restarts, display problems, or imaging misalignment during procedures. These issues could affect image quality and system reliability in clinical use.

Certain versions of Elekta's MOSAIQ oncology information system may deliver twice the intended radiation dose to cancer patients under specific conditions involving partial treatments and interrupted fields. This could occur when the system fails to verify the correct dose amount after a treatment interruption. The issue affects systems using particle therapy with certain software versions.

Philips identified that 8 Allura Xper FD20/20 X-ray systems may be missing a drip tray beneath the cooling unit due to incomplete installation or documentation during previous repairs. If the tray is not in place, coolant liquid could contact electrical components and cause a short circuit, potentially shutting down the system.