Alaska recalls

Sold nationwide. 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.

Moderate·CPSC·Apr 9, 2026·Head

Sold nationwide. 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.

Moderate·CPSC·Apr 9, 2026·Seasonal Specialties

Sold nationwide. 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.

Serious·CPSC·Apr 9, 2026·SCUBAPRO

Sold nationwide. 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.

Serious·CPSC·Apr 9, 2026·Maitys

Sold nationwide. 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.

Serious·CPSC·Apr 9, 2026·Silks

Sold nationwide. 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.

Serious·CPSC·Apr 9, 2026·Snooz

Sold nationwide. 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.

Serious·CPSC·Apr 9, 2026·Yungu

Sold nationwide. 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.

Serious·CPSC·Apr 9, 2026·Vitaquest

Sold nationwide. 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.

Serious·CPSC·Apr 9, 2026·Bissell

Sold nationwide. 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.

Serious·CPSC·Apr 9, 2026·Wybotics

Sold nationwide. 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.

Moderate·FDA·Apr 8, 2026·Blaine Labs

Sold nationwide. 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.

Moderate·FDA·Apr 8, 2026·Cardinal Health

Sold nationwide. 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.

Moderate·FDA·Apr 8, 2026·GE Healthcare

Sold nationwide. Oxoid's Microbact 12L Kit (lot 4494873) may produce ambiguous color reactions in test wells that could lead to incorrect organism identification. This affects a limited number of kits distributed in Georgia and California.

Moderate·FDA·Apr 8, 2026·Oxoid

Sold nationwide. Burlington Medical is recalling 13 radiation protective products, including thyroid shields, vests, kilts, and aprons. The shielding may weaken over time, which shortens how long the garments provide protection. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·Burlington Medical13 products

Sold nationwide. Medtronic is recalling 14 MiniMed insulin pump models, including the Paradigm, 600 series, and BLE 700 series. Changes in pump height relative to the infusion site can cause the pump to deliver too much or too little insulin. No injuries have been reported.

Serious·FDA·Apr 8, 2026·Medtronic14 products

Sold nationwide. Medline is recalling 7 kit products that contain Olympus single-use biopsy valves, totaling about 14,379 kits. Olympus found more complaints of rubber fragments detaching from a slit in the valves. A loose fragment could lodge in a patient's airway and may need to be removed in a procedure. No injuries have been reported.

Serious·FDA·Apr 8, 2026·Medline7 products

Sold nationwide. Summa Therapeutics is recalling certain Finesse BTK Multicath injectable angioplasty balloon catheters because the balloon may not meet burst strength specifications. This could cause the balloon to rupture unexpectedly during a medical procedure. The recall affects 22 units distributed in New Jersey and Florida.

Moderate·FDA·Apr 8, 2026·Summa Therapeutics

Sold nationwide. Synthes is recalling two bone screw taps, the VOLT Locking Screw Tap and the VOLT Cortex Screw Tap, because two production lots were swapped, so the taps may have an incorrect thread. The recall covers 110 units across 21 states, and no injuries have been reported.

Moderate·FDA·Apr 8, 2026·Synthes2 products

Sold nationwide. Intuitive Surgical is recalling two da Vinci S and Si reusable surgical instruments, totaling 8,247 units, after the company received complaints of frayed or broken pitch cables. The products were distributed across the U.S. and in many other countries. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·Intuitive Surgical2 products

Sold nationwide. Intuitive Surgical is recalling four reusable instrument models used with da Vinci S and Si robotic surgical systems. The company received increased complaints of broken or frayed grip cables. No injuries have been reported, and the instruments were distributed in the U.S. and in many other countries.

Moderate·FDA·Apr 8, 2026·Intuitive Surgical4 products

Sold nationwide. Olympus is recalling some SOLTIVE laser systems because a 24V power supply module may fail and make the system inoperable. The defect may also cause smoke or a burning smell, which is designed to stay inside the laser console and extinguish itself. No injuries have been reported. The recall covers 2 products, with 440 units affected, distributed in the US and several other countries.

Moderate·FDA·Apr 8, 2026·Olympus2 products

Sold nationwide. Medline Industries identified a potential breach in the sterile pouch packaging of one lot of Sterile Radiology Procedure Kits (Model DYNDH1491B). This breach may allow the kit to lose its sterile condition. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·Medline

Sold nationwide. Philips Vue Motion V12 cardiac imaging software (Product Number 1017979, software versions 12.2.0 through 12.2.8.500) may display image frames out of sequence during dynamic cine runs. This could cause medical staff to review cardiac images in the wrong order, potentially affecting diagnosis.

Moderate·FDA·Apr 8, 2026·Philips

Sold nationwide. Medline recalled two products: ENFit G-tube connectors and kits that contain them. The connectors were not made to required dimensions, so they may not seal properly with ENFit-style devices and can leak. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·Medline2 products

Sold nationwide. The surgical light assembly in Stryker CHROMOPHARE Softlit Ring systems may not adequately support the weight of the ceiling cover. This could potentially cause the cover to fall. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·Stryker

Sold nationwide. Mentor is recalling 7 product lines of breast tissue expanders, including CPX 4 US and Artoura models. The recall notice says the needle tip may be dull or blunt, which could make it hard to advance or cause it to break. No injuries have been reported. The notice refers to infusion sets, while the listed products are tissue expanders, so check the notice for details.

Moderate·FDA·Apr 8, 2026·Mentor7 products

Sold nationwide. Philips is recalling 22 models of its Allura Xper and Azurion X-ray imaging systems. The recall covers a wired foot switch that may fail to start X-ray imaging or may start it intermittently. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·Philips22 products

Sold nationwide. Siemens has recalled certain lots of its Atellica CH A1c_E hemoglobin test kit because when used with another reagent (RCRP) on the same analyzer, the A1c test may give lower-than-accurate results. Lower results could delay diabetes diagnosis or lead to inadequate treatment. This issue does not affect labs using separate analyzers for each test.

Moderate·FDA·Apr 8, 2026·Siemens

Sold nationwide. ReCor Medical distributed one Paradise ultrasound renal denervation catheter (Model PRDS-068-02, Lot M4907) that did not meet manufacturing standards and was supposed to be destroyed. The device was distributed in nine U.S. states. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·ReCor Medical2 products