State
20,082 recalls have nationwide distribution and so reach Delaware. 0 additional recalls listed Delaware specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Delaware consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
Holosun has recalled approximately 9,400 firearm dot sights with accessible lithium coin batteries that pose an ingestion hazard. The products violate federal safety regulations by lacking child-resistant packaging and required warning labels.
OdorStop Boot and Shoe Dryers and Deodorizers may pose a fire hazard due to electrical short circuits in the on-off switch. About 13,000 units have been recalled; no injuries have been reported.
About 690 Triumph TF250-X motorcycles are recalled due to plastic switch cubes that crack when exposed to brake fluid, creating electrical short circuits that can cause the motorcycle to start unexpectedly. No injuries have been reported.
Kubota is recalling approximately 2,600 MX5400DTC utility tractors due to clutch cable failure that can reduce braking power, creating a crash hazard. No injuries have been reported to date.
Homebox Blackout Roller Window Shades sold on Amazon from December 2022 to September 2024 feature long operating cords that pose strangulation and entanglement hazards to children. Consumers should place cords up and away from children.
About 900 SEJOV five-drawer dressers sold on Amazon from September 2023 through August 2024 are unstable if not properly anchored to a wall, posing tip-over and entrapment hazards to children. No injuries have been reported.
Olympus Single Use Guide Sheath Kits (models K-201 through K-204) are recalled because the radiopaque tip of the guide sheath may detach and fall into the patient during respiratory procedures.
Wismettac Asian Foods is recalling Shirakiku brand Curvee Puffs Corn Puff Snack because the product contains undeclared milk allergen. The affected product was distributed nationwide to approximately 471 consignees.
Wismettac Asian Foods is recalling Shirakiku brand Curvee Puffs Corn Puff Snacks due to undeclared milk. The product poses a serious risk to consumers with milk allergies. All lots distributed nationwide are affected.
Wismettac Asian Foods, Inc. is recalling Shirakiku brand Curvee Puffs Corn Puff Snack due to undeclared milk on the label. Consumers with dairy allergies should not consume this product.
Riverside Natural Foods is recalling Chocolate Banana Granola Bars sold nationwide due to potential metal contamination. Consumers should not eat affected products and should consult a healthcare provider if consumed.
Cardinal Health is recalling Presource Kits containing surgical strips and patties due to potential endotoxin contamination. Approximately 973,785 units were distributed in the US, Canada, and Saudi Arabia.
Cardinal Health is recalling Presource surgical kits due to potential endotoxin contamination in non-sterile surgical strips and patties. Approximately 973,785 units were distributed to the US, Canada, and Saudi Arabia.
Cardinal Health Presource Kits containing laryngoscopy packs are being recalled due to potential endotoxin contamination in non-sterile surgical strips and patties.
CareFusion recalls Pyxis medication dispensing systems due to software issues that could delay access to medications, result in incorrect doses, or allow unauthorized access.
The BD Pyxis MedStation Auxiliary 4000 medication cabinet may experience drawer and door failures, potentially delaying medication access in healthcare facilities.
Integra LifeSciences is recalling MediHoney Gel Wound & Burn Dressing Gel (Model 31815) due to potential induction seal defects in the tube packaging. Approximately 12,166 units were distributed worldwide, including throughout the United States and Malaysia.
The FDA is recalling BD Pyxis MedStation ES medication cabinets due to potential drawer and door failures that could delay medication access. Affected healthcare facilities should check their devices and contact the manufacturer if malfunctions occur.
Microbiologics Inc is recalling HPV verification test panels (REF 8235) due to quality control failures that allowed defective units to be released. The panels may produce invalid test results or fail to detect HPV.
Cardinal Health Presource Kits for robotic urology surgery are being recalled due to potential endotoxin contamination in surgical strips and patties. No adverse events have been reported.
Microbiologics is recalling a lot of HPV diagnostic control materials due to inadequate quality control during release. The control's HPV 16 L1 concentration is too low, potentially causing test failures and invalid results in clinical laboratories.
Murata Vios, Inc. is recalling the Vios Monitoring System Bedside Monitor, Model BSM2050, due to premature failure of the pulse oximeter SpO2 sensor. When the sensor fails, the system displays an incorrect warning that may mask the actual monitoring problem.
Riverside Natural Foods is recalling Mixed Berry Granola Bars nationwide (2.4 million cases) because they may contain metal pieces. Affected consumers should not eat the product and should contact the manufacturer for a refund.
Cardinal Health is recalling Presource Kits (surgical strips and patties used in ophthalmic procedures) due to potential endotoxin contamination in non-sterile components.
Hologic is recalling 55,335 Sertera-14 biopsy devices nationwide because the inner needle can separate from the hub, creating a risk of needle dislodgement during use.