State
72,971 recalls have nationwide distribution and so reach Delaware. 3,435 additional recalls listed Delaware specifically in their distribution scope.
Of the 3,435 recalls naming Delaware we have scored against our rubric, 477 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 937 (27%) are Severe.
Which agencies issued them
These figures cover only the 3,435 recalls whose distribution notice names Delaware specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 545 LuckupShein window roll up shades sold on SHEIN.com have long operating cords that pose strangulation and entanglement hazards to children. The shades violate federal window covering regulations.
Deals Oasis recalls Kids Thrill Shape Sorter Car Toys because the included balls violate small-parts regulations for children under three and pose a choking hazard. No injuries have been reported.
Kawasaki Motors is recalling about 3,400 model year 2025 KX series competition and cross-country motorcycles because the primary gear for the crankshaft can fail, creating a crash hazard. No injuries have been reported.
Huffy Corporation recalled about 24,700 Torex 24V ride-on UTVs due to improper wiring that can cause overheating, smoking, and fires. The company has received 20 incident reports including five minor burns.
Huffy is recalling approximately 23,260 children's 12-volt ride-on Tonka Dump Trucks because the controller can overheat, posing fire and burn hazards. Consumers should stop using the trucks immediately and contact Huffy for a free replacement controller.
BTAMREE roll up window blinds sold on Amazon.com are being recalled because their long operating cords pose a strangulation and entanglement hazard that can cause serious injury or death to children. Consumers should stop using the product immediately and contact BTAMREE for a refund.
Sondiko Butane Torches lack required child-resistant mechanisms and violate federal multipurpose lighter regulations, posing a risk of serious burn injuries or death to children. About 33,650 units were sold on Amazon from October 2023 through March 2025.
International is recalling certain 2025-2026 HV, HX, LT, MV, RH and 2025 EMV vehicles because the linkage connecting the right-side wiper arm to the motor may separate, causing the wipers to fail.
Baxter Healthcare is recalling Welch Allyn Connex Vital Signs Monitors because some units experienced battery-related fires caused by unapproved third-party after-market batteries.
Dr. Reddy's Laboratories is recalling Levetiracetam 0.75% Sodium Chloride Injection due to a labeling discrepancy where the infusion bag is incorrectly labeled as 0.82% Sodium Chloride 500 mg/100 mL instead of the correct 0.75% Sodium Chloride 1,000 mg/100 mL.
Avanos Medical is recalling Ballard Closed Suction Catheters (Model 220135) due to lack of sterility assurance. The recall affects 9,020 units distributed nationwide and internationally.
Thoratec LLC is recalling HeartMate Mobile Power Units due to an electrical component defect that may prevent the unit from turning on, cause unprompted shut down, or trigger false alarms. If power is lost and not switched to rechargeable batteries within 15 minutes, the connected pump may lose power.
Avanos Medical is recalling 1,420 units of Ballard Closed Suction Catheters (Model 2271418-5) due to lack of sterility assurance. The affected product was distributed worldwide, including across the US and internationally.
Ford is recalling 2022-2023 F-150 Lightning vehicles because loose battery fasteners may cause electrical arcing, increasing the risk of fire or loss of drive power.
Baxter Healthcare is recalling the Welch Allyn CONNEX Accessory Power Management Stand due to reports of battery-related fires caused by unapproved third-party batteries.
Avanos Medical is recalling Ballard Closed Suction Catheters (Model 22714183-5) due to lack of sterility assurance. The affected lot was distributed nationwide and internationally.
Avanos Medical is recalling Ballard Closed Suction Catheters (Model 20083) due to lack of sterility assurance. The company has distributed approximately 9,960 units worldwide.
Avanos Medical is recalling Ballard Closed Suction Catheters (Model 2210-5) because they lack adequate sterility assurance. The recall affects approximately 2,080 units distributed worldwide, including across most US states and several countries.
Channel Medsystems is recalling the Cerene Cryotherapy Device (Model FGS-7000) due to a defective evaporator gasket that may fail to seal, causing liquid nitrous oxide to leak during or after treatment.
Marketside brand celery sticks (1.6 oz) have been recalled due to Listeria monocytogenes contamination. Duda Farm Fresh Foods, Inc. is recalling approximately 1,587 cases distributed nationwide.
Baxter Healthcare is recalling Welch Allyn CP150 Electrocardiographs worldwide due to reports of battery-related fires. The fires occurred when devices used non-approved, third-party aftermarket batteries.
Bard Access Systems is recalling BD 4 Fr Single-Lumen PowerPICC Catheters worldwide because tubing material may exceed specifications, causing leaks and potentially serious complications including infection and air embolism.
Avanos Medical is recalling Ballard Closed Suction Catheters (Model 198, 8 F, Y-Adapter) for neonates and pediatrics due to lack of sterility assurance. The recall affects 1,980 units distributed nationwide and internationally.
Avanos Medical is recalling Ballard Closed Suction Catheters (Model 210, 10 F Elbow) for neonates and pediatric patients due to lack of sterility assurance. Approximately 4,000 units were distributed worldwide.
Avanos Medical is recalling Ballard Closed Suction Catheters (Model 227-5) due to lack of sterility assurance. The recall affects 1,040 units distributed nationwide and internationally.