State
72,919 recalls have nationwide distribution and so reach Maine. 3,894 additional recalls listed Maine specifically in their distribution scope.
Of the 3,894 recalls naming Maine we have scored against our rubric, 468 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 791 (20%) are Severe.
Which agencies issued them
These figures cover only the 3,894 recalls whose distribution notice names Maine specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Silks-branded children's loungewear sets are recalled because they violate mandatory flammability standards for children's sleepwear. About 7,900 units are affected.
Akron Brass is recalling Enovation Controls PowerView 700 displays that may fail to power on or respond to touch, preventing the activation of emergency lights and equipment.
Chrysler is recalling 2026 Jeep Wrangler vehicles because insufficient child seat tether welds may reduce restraint effectiveness during a crash.
Chrysler is recalling 2025–2026 RAM 1500, 2500, 3500, 4500, and 5500 vehicles due to a software error that may cause the instrument panel display to fail, hiding critical safety information like gear selection and warning lights.
Muscccm pool drain covers are recalled because they violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act, posing entrapment and drowning hazards.
Happiness Light LED lights are recalled because their lithium coin batteries can be accessed easily by children, posing an ingestion hazard. About 2,800 units are affected.
Male-to-male extension cords sold on Walmart.com are recalled because their exposed prongs can become energized when one end is plugged into a generator, posing an electrocution risk.
ShymeryDirect LED lights are recalled because their lithium coin batteries can be accessed easily by children, posing an ingestion hazard. About 295 units are affected.
One lot of Magnesium Sulfate in Water for Injection is being recalled after a foil pouch labeled as magnesium sulfate was found to contain an IV bag of tranexamic acid.
Philips Respironics is recalling the Trilogy Evo Universal ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
Philips Respironics is recalling the Trilogy Evo ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
Philips Respironics is recalling the Trilogy EV300 ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
Philips Respironics is recalling the Trilogy Evo O2 ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
Burlington Medical is recalling BAT (Breast, Axilla and Thyroid) Coverage because of the potential for attenuation degradation over time.
Medtronic is recalling MiniMed 770G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Cardinal Health is recalling two lots of Monoject Tuberculin Syringes because the packaging identifies them as 1 mL Luer Lock tuberculin syringes but the contents are U-100 insulin syringes.
JFE Franchising Inc is recalling Dumpling Vegetable and Loaded Dumpling Vegetable products due to the presence of glass fragments. The products were distributed across multiple U.S. states.
Medline is recalling four bronchoscopy and laryngoscopy kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
K.C. Pharmaceuticals is recalling Sterile Eye Drops Soothing Tears, sold as Rugby Lubricating Eye Drops and Walgreens Lubricant Eye Drops, for lack of assurance of sterility.
Leader Ultra Lubricating Eye Drops, containing polyethylene glycol 400 and propylene glycol, are being recalled for lack of assurance of sterility.
Philips is recalling the Allura Xper FD20/15 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Intuitive Surgical is recalling da Vinci S and Si Tenaculum Forceps Instruments following increased complaints regarding frayed or broken pitch cables on reusable surgical instruments.
Medtronic is recalling MiniMed 740G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Philips is recalling the Allura Xper FD10 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Philips is recalling the Azurion 7 B12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.