State
73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Nissan recalls 2021 INFINITI QX50 and other vehicles due to front steering knuckles and rear axle housings with insufficient strength from improper heat treatment, which could deform on impact and cause loss of steering control or wheel separation.
Triple E Recreational Vehicles is recalling 2020-2021 Serenity, Unity, and Wonder models because a low-positioned metal deflector allows exhaust to char the wood frame, increasing fire risk.
Chrysler is recalling RAM trucks because incorrect manual torque specifications can cause wheel studs to over-tighten, break, and lead to wheel separation and possible crashes.
Umbrosa is recalling about 250 pool and patio umbrellas because the arm can break at the elbow while in use, posing an injury hazard.
Williams Advanced Materials & Chemicals is recalling sodium hydroxide, heptane, and naphtha because the packaging is not child-resistant and labels violate federal requirements.
Temsa is recalling 276 vehicles because a sealing washer defect may cause high-pressure fuel leaks, increasing the risk of fire.
Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate dietary supplements because FDA inspections found undeclared milk, wheat, and soy.
Simkins Brothers Sweets is recalling Natural Way Almond Butter due to potential undeclared peanuts. Consumers should check for lot #505721.
Biopsybell S.R.L. is recalling 250 units of 10 Gauge Cement Delivery Cannulas labeled as sterile but potentially not sterilized.
Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate dietary supplements because FDA inspections found undeclared milk, wheat, and soy.
Daimler Trucks North America is recalling 2019 Freightliner M2 Business Class vehicles with 14Xe ePowertrains because insufficiently crimped stator wires may cause overheating and loss of drive power.
Biopsybell is recalling 160 units of 11G Direct Single Delivery kits because they were labeled as sterile but may not have been sterilized.
Teva Pharmaceuticals is recalling Methylprednisolone Acetate Injectable Suspension due to a lack of assurance of sterility.
Biopsybell is recalling 50 units of 11G Direct Single Access devices labeled as sterile but potentially not sterilized, distributed in Mississippi and Kentucky.
Teva Pharmaceuticals is recalling specific lots of Haloperidol Decanoate Injection because the company cannot guarantee the product is sterile.
Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate Honey Granola dietary supplements because they contain undeclared milk, wheat, and soy.
Thor Motor Coach is recalling certain 2022 Sequence, Rize, Scope, and Tellaro recreational vehicles. The Flex-190 solar panel junction box may experience electrical shorts, increasing the fire risk.
Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate Cookies N Cream dietary supplements because the product contains undeclared milk, wheat, and soy.
Hi-Tech Pharmaceuticals is recalling Precision Protein Cookies & Cream because it contains wheat but is labeled as "Gluten Free".
Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate Strawberry Milkshake dietary supplements because they contain undeclared milk, wheat, and soy.
Hyobin LLC is recalling Triple SupremeZen Plus 3500 capsules because FDA analysis found the unapproved drug tadalafil. The product was marketed without an approved NDA or ANDA.
Hyobin LLC is recalling PremierZen Black 5000 capsules because FDA analysis detected the unapproved drug tadalafil. The product was marketed without an approved NDA or ANDA.
Biopsybell S.R.L. is recalling 625 units of 10 Gauge Direct Unilateral Stylets because they were labeled as sterile but may not have been sterilized.
Hyobin LLC is recalling PremierZen Extreme 3000 capsules because FDA analysis found the unapproved drug tadalafil. The product was marketed without an approved NDA or ANDA.
HSN is recalling 5.4 million Joy/JM-branded My Little Steamer handheld clothing steamers because they can expel hot water, posing a serious burn hazard.