State
73,596 recalls have nationwide distribution and so reach Delaware. 3,438 additional recalls listed Delaware specifically in their distribution scope.
Of the 3,438 recalls naming Delaware we have scored against our rubric, 475 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,112 (32%) are Severe.
Which agencies issued them
These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Kia is recalling 2020-2024 Telluride vehicles because the front power seat motor may overheat, posing a fire risk while parked or driving.
Cooper Lighting recalls about 42,000 Metalux Optimized High Bay LED light fixtures due to a fire hazard. The LED board can overheat or contact combustible materials; nine fires have been reported with no injuries or property damage.
Crestline Coach is recalling 2026 Ford CCL166 Type III ambulances because a bolt may puncture the fuel line, creating a fire hazard.
Jayco is recalling 2026 Heartland Cyclone travel and fifth-wheel trailers because the inverter may lack a grounding connection, posing fire and shock risks.
Kia is recalling 2022-2024 EV6 and 2024 EV9 vehicles because high voltage battery cells may contain misaligned electrodes, creating a fire hazard.
Hyundai is recalling 2023-2024 Ioniq 5 vehicles because high voltage battery cells may contain misaligned electrodes, posing a fire risk while parked or driving.
Rowenta is recalling cordless vacuum cleaners with lithium-ion batteries that can overheat and ignite, posing a risk of fire and burn injury. About 3,660 units are affected; no injuries have been reported.
Warn Industries is recalling Wireless Remote Kits (part numbers 90287 and 90289) because the remote control may be incompatible with legacy winches, causing unexpected movement and increasing injury risk.
AMASKY Nursing Pillows, sold on Amazon from January to March 2026, violate safety standards and can obstruct infant breathing, posing a serious risk of suffocation. No injuries have been reported.
Topyond pool drain ports with covers violate federal entrapment protection standards and pose serious injury or death risks from entrapment and drowning. Consumers should stop using pools with these drain ports immediately.
Winco Fireworks International recalls Unity 7 Shot 200 Gram Aerial Cake firework devices that can tip over, creating risk of serious injury from explosion and burns. About 87,120 units sold at Pyro City and independent fireworks stores nationwide from January through May 2026 are affected.
Altec is recalling 2022-2026 Service Body vehicles because inverter AC wiring may be damaged, creating a short circuit and fire risk.
CPSC has recalled POPOOO Jungle Safari LED Finger Lights sold on Amazon because the toys contain easily accessible button cell batteries that can cause serious injury or death if swallowed. No injuries have been reported.
Target has recalled approximately 49,000 Gigglescape Under the Sea Popping Toys because the clear plastic dome can detach, exposing small plastic balls that pose a choking hazard. One child began to choke after the dome detached.
Winco Fireworks International is recalling Roman Candles 8 Shot 3-Pack firework devices because the fireworks can malfunction and shots can blow out the side of the tube, posing a risk of serious injury from explosion and burn hazards. No injuries have been reported.
CareFusion 213, LLC is recalling ChloraPrep One-Step (chlorhexidine gluconate and isopropyl alcohol) due to wrinkles in the paper lidding that may breach the seal, compromising sterility assurance.
Intuitive Surgical recalls certain Da Vinci surgical system operative components due to a defective E-brake retainer pin that may fail to engage the E-brake, potentially causing uncontrolled motion and patient injury.
Medline Industries recalled multiple convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance. The company identified these modifications and notified the FDA of the deviation from the approved 510(k) design.
Abiomed is recalling certain Impella CP Set with SmartAssist (10th Generation) units with affected 14Fr Low Profile Introducer Kits due to potential for thrombus (blood clot) formation during prolonged use.
Spring & Mulberry Inc. is recalling Blood Orange Date-Sweetened Chocolate bars due to potential Salmonella contamination. Affected products were distributed nationwide.
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside FDA-cleared specifications. The recall affects approximately 113,843 kits distributed nationwide.
Abiomed is recalling 3 units of the 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP due to potential for blood clot formation during prolonged use.
Spring & Mulberry Inc. is recalling Earl Grey Date-Sweetened Chocolate bars due to potential Salmonella contamination. The affected product was distributed nationwide.
Surgify Medical is recalling Surgify Halo 4.0 mm Extendable surgical burrs due to potential breakage during bi-portal endoscopic spinal surgery. The breakage could create a safety hazard during the procedure.
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance.