State
72,820 recalls have nationwide distribution and so reach Delaware. 3,434 additional recalls listed Delaware specifically in their distribution scope.
Of the 3,434 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 936 (27%) are Severe.
Which agencies issued them
These figures cover only the 3,434 recalls whose distribution notice names Delaware specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Jayco is recalling 2026 Entegra Anthem motorhomes because the vehicle certification label may list the wrong tire size, which could lead to installing incorrect replacement tires.
Midwest Industries is recalling 2027 Yamaha boat trailers because the tongue may fail during towing, causing the trailer to detach and increasing crash risk.
ARBOC is recalling 2017-2026 Spirit of Independence transit buses because incorrect washers on rear spring hanger bolts may cause the hanger to detach, increasing crash risk.
Mercedes-Benz USA, LLC is recalling certain 2020-2026 Mercedes-Benz vehicles because a faulty door lock micro-switch may cause the vehicle to roll away.
Frontrunner is recalling 2025 transit buses because wheelchair retractors may fail to lock, increasing injury risk. Owners will be notified to have parts replaced.
CuddleCubs Creations Baby Highchair Teething Toy Sets are recalled due to pull-string teething toys that violate mandatory toy safety standards. The silicone strings can lodge in a child's throat, creating a risk of choking and respiratory distress.
BMW is recalling certain 2020-2026 S 1000 RR motorcycles because vibration may cause ignition lock failure, leading to engine stalls or electrical system failures.
Romorgniz 12-Drawer Fabric Dressers sold on Amazon pose tip-over and entrapment risks to children if not anchored to the wall. About 10,040 units are affected.
About 670 Sviyatp pool drain covers sold online violate federal safety standards and pose entrapment and drowning hazards. Consumers should stop using affected pools immediately and contact Sviyatp for a refund.
K&N Engineering is recalling specific K&N and Spectre replacement fuel filters because the O-ring may disintegrate, causing leaks or clogs.
EnHomee 9-Drawer Fabric Dressers sold on Walmart.com pose a risk of serious injury or death from tip-over and entrapment if not anchored to the wall. About 16,809 units are affected.
Aojieni Silicone is recalling about 5,918 Sili Factory Pull String Teething Toys because the silicone strings violate toy safety standards and can lodge in a child's throat, posing a serious choking risk.
Peony Design has recalled personalized baby bibs and stroller bags sold online because snaps can detach, posing a choking risk to young children. The company is offering refunds.
OeyUoc white pool drain covers sold on Amazon violate safety standards and pose entrapment and drowning risks. About 404 units have been recalled; consumers should stop using them immediately.
Forest River is recalling 2026-2027 Pause and OG Luxury Coach RVs because a rooftop fan circuit board may overheat and cause a fire.
Forest River is recalling 2027 travel trailers because the Federal Placard may list an incorrect fresh water tank capacity, which could lead to vehicle overloading.
Argon Medical Devices is recalling General Biopsy Tray kits containing Lidocaine HCL Injection because the kits do not meet sterility release criteria.
Abiomed, Inc. is recalling ABIOMED Intro Kit heart pump introducer sheaths due to potential leakage from under the sheath cap and along hub score lines. The manufacturing defects are not visually detectable by users.
Argon Medical Devices is recalling T-Lok Bone Marrow Tray kits containing Lidocaine HCL Injection USP 1% because the kits did not meet sterility release criteria.
Olympus Corporation of the Americas is recalling the Olympus Ellik Evacuator (Model 194) worldwide because certain sterilization parameters in the instructions may not render the device adequately sterile.
ICU Medical is recalling Plum Duo Infusion Pump v1.2.3 units due to a software defect that may cause the pump to deliver up to twice the programmed volume without decrementing the display, risking patient overdose.
Medtronic is recalling its Bio-Medicus Adult Cannula Kit (Product Number 96530-115) used in cardiopulmonary bypass procedures due to the discovery of loose foreign material containing trace levels of blood in two units.
ICU Medical is recalling the Plum Solo Precision IV Pump (v1.0.3) because in specific scenarios, the pump may fail to decrease the displayed volume and could deliver up to twice the programmed medication amount.
Abiomed is recalling ABIOMED Insertion Kits due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines. The manufacturing defect is not visually detectable by users.
Abiomed is recalling the Impella RP Flex heart pump due to potential introducer sheath leakage from the sheath cap and hub score lines. The manufacturing defect is not visually detectable.