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.
Tenneco Automotive is recalling NAPA steering inner tie rod ends for certain Ford C-Max, Escape, and Focus models because the stud may separate, causing a loss of steering.
Zoox is recalling Automated Driving Systems because software may fail to detect heavy smoke, increasing crash risk in low-visibility areas.
About 1,400 Flaunt MagSafe Battery Chargers (model E33A) are being recalled because the lithium-ion battery can overheat and ignite. The company has received five reports of the power banks catching fire, including two reports of burns and four reports of property damage.
Volvo Trucks is recalling certain 2026 VNL, VNR, VHD, VN, and VAH vehicles because the steering arm may not be tightly fastened to the steering knuckle, risking loss of steering control and crashes.
Moodooy Adult Portable Bed Rails sold on Amazon violate mandatory safety standards and pose risk of entrapment and asphyxiation. The rails lack required warning labels and users can become trapped within the rail or between the rail and mattress.
BBRKIN and MouTec biometric firearm safes can be opened by unauthorized users, creating a serious injury and death risk. Consumers should immediately stop using the biometric feature and use the key only.
Greenworks Tools recalls Kobalt yard power tools with USB-C batteries due to risk of fire when batteries are charged via the USB-C port while inserted in the tool. The firm received 34 reports of batteries smoking, sparking, or catching fire, with no injuries reported.
Conair is recalling the Cuisinart Propel+ Four Burner 3-in-1 Gas Grill because the tempered glass window in the pizza oven can shatter during use, posing a laceration risk. About 12,660 units were sold.
Best Buy is recalling about 3,820 Insignia Front Control Gas Ranges because the front-mounted knobs can be accidentally activated by humans or pets, creating a fire hazard risk.
WonderStone Infant Walkers sold on Walmart.com violate mandatory infant-walker standards because they can fit through doorways and fail to stop at steps, posing a risk of serious injury or death from falls. No injuries have been reported.
Insulet Corporation is recalling Omnipod DASH Pods worldwide due to external soft cannula damage during manufacturing that can cause insulin to leak around the pod instead of being delivered. This may lead to high blood glucose levels and, in severe cases, diabetic ketoacidosis or death.
BMW is recalling 29,119 vehicles because a corroded starter relay may overheat and short circuit, increasing the risk of a fire.
CareFusion 213, LLC is recalling ChloraPrep One-Step applicators because unsterilized units intended for further processing were distributed to customers outside the intended distribution channel, creating a lack of sterility assurance.
Asclemed USA Inc. is recalling specific lots of Accucaine (Lidocaine HCl Injection USP, 1%) distributed nationwide due to lack of assurance of sterility. The affected product is distributed by Enovachem Pharmaceuticals.
A M S Preop Kit-NS surgical convenience kits are being recalled due to contamination with Paenibacillus phoenicis bacteria discovered during sterilization testing. The kits were distributed nationwide in PA, GA, CA, and WA.
Insulet Corporation is recalling Omnipod (Eros) Pod units due to external soft cannula damage during manufacturing that can cause insulin leakage instead of delivery to the user. High blood glucose levels and serious complications including diabetic ketoacidosis (DKA) or death may result from under-delivery of insulin.
Accord BioPharma is recalling IMULDOSA (ustekinumab-srlf) Injection due to lack of assurance of sterility. The affected lot was distributed nationwide.
BMW of North America, LLC is recalling various BMW and Toyota Supra models because the engine starter may overheat and catch fire.
Baxter Healthcare Corporation is recalling the Hillrom VOLARA P.CIRCUIT 5KIT medical device due to reports of air and medication leakage from the nebulizer cup, which can reduce oxygen levels and compromise medication delivery.
CareFusion 213, LLC is recalling ChloraPrep One-Step applicators distributed nationwide because unsterilized units intended for further processing were shipped to customers outside the intended distribution channel.
Windstone Medical Packaging is recalling 1,080 DSAEK Pack-RX surgical convenience kits containing Webcol Large Alcohol Prep Pads contaminated with Paenibacillus phoenicis bacteria discovered during a sterilization audit.
Baxter Healthcare is recalling Hillrom VOLARA System patient circuits due to reports of air and medication leakage from the nebulizer cup, which can reduce oxygen levels and prevent proper medication delivery.
Cipla USA, Inc. is recalling Cinacalcet Hydrochloride 90 mg tablets (Lot #5PB0563, expiring 4/30/2027) distributed nationwide due to the presence of N-nitroso-cinacalcet above acceptable daily intake levels, a manufacturing deviation.
W. L. Gore & Associates is recalling 467 GORE TAG Thoracic Branch Endoprosthesis Side Branch Components worldwide due to risk of catheter separation during deployment.
Accuray Incorporated is recalling Cyberknife Treatment Delivery Systems equipped with the Xchange Robotic Collimator Changer due to a risk that the collimator may not fully dock and could fall from the housing if the in-room control pendant is used.