State
73,503 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 1,110 (32%) are Severe.
Which agencies issued them
These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Indian Motorcycle is recalling 2020 Scout Bobber Sixty models because an ECU update may have disabled brake lights, increasing crash risk.
Starcraft is recalling certain 2021-2022 recreational vehicles with defective Winntec propane regulators that may fail, causing increased pressure and larger flames in gas appliances, raising fire risk.
Honda is recalling 2019-2020 CB500X and CBR500R motorcycles because excessive grease in the ABS modulator may cause a brake fluid leak, increasing crash risk.
Jayco is recalling certain 2017-2022 recreational vehicles with Winntec propane regulators that may fail and increase propane pressure, raising the risk of fire in gas appliances.
Cardinal Health recalls 267 million Monoject 0.9% Sodium Chloride Flush Syringes due to a plunger defect that may reintroduce air into the syringe, posing a risk of air embolism during IV administration.
Custopharm, Inc. is recalling Fludarabine Phosphate for Injection, USP 50 mg because the manufacturer detected microbial contamination during environmental monitoring in aseptic manufacturing areas, raising sterility assurance concerns.
Cardinal Health is recalling Monoject 0.9% Sodium Chloride Flush Syringes because the plunger may draw back after use and reintroduce air into the syringe.
SterRx is recalling Sodium Bicarbonate in 5% Dextrose Injection (1,000 mL bags) nationwide due to lack of assurance of sterility. Patients using affected lots should consult their healthcare provider immediately.
SterRx is recalling Sodium Bicarbonate in 5% Dextrose Injection due to microbial contamination confirmed by third-party laboratory testing. The affected product is a prescription intravenous injection distributed nationwide.
Mack is recalling 2020-2022 MD trucks because a defective cotter pin may leave the brake pedal unsecured, increasing crash risk.
Cardinal Health Monoject flush syringes may have a defect allowing the plunger to draw back and reintroduce air into the syringe. The FDA issued a Class I recall for over 267 million units distributed nationwide.
Eli Lilly & Company is recalling Trulicity (dulaglutide) 0.75 mg autoinjector pens because some contain double the labeled strength. Affected patients may receive an incorrect dose.
KVK-Tech, Inc. is recalling Atovaquone Oral Suspension due to temperature abuse that caused unusual grittiness in the product. The defect may affect the medication's quality and safety.
Cahills Farm Cheese Limited is recalling Cahills Ireland Whiskey Cheese 5lb. Waxed Deli Wheels due to potential Listeria monocytogenes contamination. The affected product was distributed nationwide.
Cahills Farm Cheese Limited is recalling Cahills Ireland Red Wine - 5 lbs. Waxed Deli Wheel cheese nationwide because it may be contaminated with Listeria monocytogenes, a serious foodborne pathogen.
Cahills Farm Cheese Limited is recalling Cahills Ireland Original Irish Porter cheese products due to possible Listeria monocytogenes contamination. The recall affects approximately 4.4 tons distributed nationwide.
Lidl Preferred Selection Irish Stout Cheddar cheese may be contaminated with Listeria monocytogenes. Affected products were distributed nationwide and should not be consumed.
Cahills Farm Cheese Limited is recalling Lidl Preferred Selection Red Wine Cheddar cheese due to potential Listeria monocytogenes contamination. Consumers should not eat this product.
Porsche is recalling 4,934 vehicles because rear-axle carrier side sections may fracture, potentially causing loss of control and increasing crash risk.
HIS ENTERPRISE INC is recalling all lots of Miss Slim capsules (10-count and 30-count boxes) distributed nationwide in the USA because the product was marketed without required FDA approval (ANDA/NDA).
A Philips Ingenia MRI system has been recalled due to installation of a 42 psi pressure relief valve instead of the correct 3.75 psi valve, which may result in helium gas release and injury.
Philips Ingenia Elition X MRI systems contain an incorrectly installed pressure relief valve that may release helium gas and cause injury. The recall affects 6 U.S. units and 12 units distributed internationally.
Roche Diabetes Care is recalling Accu-Chek Inform II glucose test strips because vials may open during shipment, exposing strips to humidity and potentially causing inaccurate test results.
Roche is recalling Accu-Chek SmartView Test Strip vials that may open during shipment. The vials can be exposed to humidity, damaging the strips and potentially causing inaccurate glucose readings.
Roche Diabetes Care is recalling Accu-Chek Aviva Plus Test Strips because vials may open during shipment, exposing strips to humidity and causing inaccurate glucose readings that could lead to improper treatment decisions.