State
73,100 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, 477 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 939 (27%) are Severe.
Which agencies issued them
These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Brompton T-Line Foldable Bicycles are recalled because loose steerer clamp bolts can cause misalignment between the handlebar and front wheel, risking loss of steering control and falls. About 1,080 units are affected.
Chrysler is recalling certain 2021 Jeep Wrangler and Gladiator vehicles due to a powertrain control module software defect that may cause engine stall, resulting in loss of drive power and increased crash risk.
The left rear seat back in certain 2023 Dodge Challengers may not lock in the upright position, increasing the risk of injury in a crash. Dealers will inspect and adjust the seat latch free of charge.
RH Baby & Child is recalling about 480 Jeune French Contemporary Upholstered Panel Cribs because cylindrical metal inserts in the wooden frame can become loose and detach, posing a choking hazard to infants.
The left rear seat back in certain 2023 Dodge Charger vehicles may not lock in the upright position. This creates a risk of injury in a crash.
About 55,480 Avocado Organic Cotton Mattress Pad Protectors are being recalled because they violate the federal flammability regulation for mattress pads, posing a fire hazard. No injuries have been reported.
Lowe's has recalled about 27,400 Origin 21 oval and rectangle black framed wall mirrors because they can detach from their metal hanging plates and fall, creating laceration and impact hazards. The company has received 15 reports of separation with no injuries yet reported.
Papablic Archie Infant Swings (model PAPABLIC61A) pose a suffocation risk because they are designed for infant sleep with an incline angle greater than 10 degrees, violating federal safety regulations. Consumers should stop using them immediately.
Peace Industry Group is recalling about 1,000 Peace Sports Youth All-Terrain Vehicles due to violations of federal ATV safety standards. The ATVs have defective handlebars, faulty parking brakes, missing reflectors, and footguards that pose risks of laceration, amputation, and collision.
Beberoadlove is recalling about 1,940 New Moon Travel Bassinets because they lack a required stand and can fall from elevated surfaces, violating federal safety regulations for infant sleep products. No injuries have been reported.
Daimler Trucks North America is recalling 2024-2025 Thomas Built Buses Saf-T-Liner C2 and C2 Jouley school buses because an improperly installed air conditioning ground cable may overheat and cause a fire.
General Motors is recalling 2024 Chevrolet Malibu vehicles that may have an incorrect owner's manual. The wrong manual could contain inaccurate vehicle safety information.
Medtronic Xomed is recalling NIM Vital Nerve Monitoring systems because they may fail to detect nerve damage or dysfunction. Approximately 7,804 units were distributed worldwide.
Jayco is recalling 2025 Entegra Cornerstone motorhomes because inadequate fuse protection on chassis batteries increases the risk of a fire.
Embecta Corp. is recalling BD Nano 2nd Gen Pen Needles that were distributed at or after their February 29, 2024 expiration date. Using expired needles cannot guarantee sterility and integrity.
Medtronic is recalling 636 units of TourniKwik Tourniquet Sets due to incorrect components placed in four manufactured lots. Distribution includes the US states of Minnesota, Massachusetts, Utah, California, Florida, Japan, and Slovenia.
The Abbott Infinity 7 implantable pulse generator's replacement indicator and end-of-service date may be shorter than the product labeling states, potentially leading to loss of therapy for patients.
B Braun is recalling Perfusor Space syringe pumps because manufacturing changes to Cardinal Health Monoject syringes may cause incompatibility, resulting in dosing errors or delayed treatment.
Olympus is recalling 86 ESG-410 Electrosurgical Generators because they may fail to power on during use, potentially delaying treatment or prolonging surgery.
Abbott is recalling 1198 Infinity 7 Implantable Pulse Generators due to potentially incorrect service life indicators and end-of-service dates in product labeling, which could result in loss of therapy.
B Braun's Perfusor Space infusion pump may be incompatible with Cardinal Health Monoject syringes affected by manufacturing changes, creating risks of overdose, underdose, and delayed therapy.
B Braun is recalling Perfusor Space infusion pump kits because Cardinal Health Monoject syringes have manufacturing changes that make them incompatible, potentially causing overdose, underdose, or delayed therapy.
Beckman Coulter is recalling 143 Dxl 9000 Immunoassay Analyzers due to nonconforming USB cables with brass instead of gold contacts. Brass may corrode, potentially disabling internal communication and delaying patient test results.
Abbott Infinity 5 implantable pulse generators have inaccurate end-of-service dates in labeling, which may result in loss of therapy. Approximately 5,900 units are affected and distributed worldwide.
Abbott is recalling 5,900 Infinity 5 implantable pulse generators because the replacement indicator and end-of-service date may be shorter than labeled, potentially causing premature device failure. Patients should contact their doctor about device status.