State
73,486 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 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
American Honda is recalling about 1,400 Honda Pioneer 700, Pioneer 1000, and Talon 1000 recreational off-highway vehicles equipped with electric power steering. The vehicles can lose steering function, posing crash and injury hazards.
Amazon is recalling about 15,300 AmazonBasics Memory Foam Mattresses sold between April 2020 and March 2021 because they fail to meet federal flammability standards, posing a fire hazard. No injuries have been reported.
Toyota is recalling 2018-2019 Camry vehicles because a vacuum pump component may break, causing a sudden loss of braking assist and increasing crash risk.
Sutphen is recalling 2020 Fire trucks because pressure in the power steering pump may break the shaft seal, causing a loss of steering assist and increasing crash risk.
Volkswagen is recalling certain 2021 Atlas and 2020-2021 Cross Sport vehicles whose air conditioning drain tube can become blocked, allowing water to damage the air bag control module and potentially trigger inadvertent air bag deployment.
Simply Delicious, Inc. is recalling Bobo's Almond Butter Protein Bars (2.2 oz.) because they contain undeclared peanuts, posing a risk to consumers with peanut allergies.
Jayco recalls certain 2021-2022 motorhomes with defective seat belt retractors that may fail to secure child restraint systems during crashes. Dealers will replace the retractors free of charge.
Zhejiang Kindly Medical Devices is recalling Henry Schein Safety Blood Collection Needles due to potential difficulty activating the safety mechanism. Affected lot numbers distributed nationwide.
Daimler Trucks North America is recalling Freightliner 108SD, 114SD, Coronado, and Western Star trucks from model years 2012-2022 due to unapproved tires and rims that do not meet federal safety standards.
McKesson PREVENT HT Safety Winged Blood Collection Needles may have difficulty activating their safety mechanism. The recall affects units distributed nationwide.
Z-Medica is recalling 2400 units of QuikClot Combat Gauze due to potential packaging seal failures that could compromise sterile barrier integrity. Affected lot 12645 was distributed nationwide.
Philips Azurion Interventional X-Ray Systems (software 2.1.x) may experience imaging lock-up when operators simultaneously press both the APC and Float Tabletop buttons.
Nationwide recall of McKesson PREVENT HT Safety Blood Collection Needles (22G 1 1/4 inch) due to potential difficulty activating the safety mechanism. The protective feature may fail to engage properly during use.
McKesson PREVENT HT Safety Blood Collection Needles are being recalled due to potential difficulty in activating the safety mechanism. The recall affects needles distributed nationwide, including specific lot numbers with expiration dates through May 2025.
Toyota is recalling 2022 Sienna and Sienna Hybrid vehicles with eight-passenger seating because an incorrect seat belt webbing guide may cause the belt to tear during a crash.
McKesson PREVENT HT blood collection needles with specific lot numbers may have difficulty activating their safety mechanism. Healthcare facilities should contact the manufacturer for replacement guidance.
Baxter's Hemodialysis Delivery System may incorrectly revert to old prescription values when operators change prescriptions after filter changes, potentially resulting in incorrect treatment parameters.
Henry Schein safety blood collection needles may have difficulty activating their safety mechanism, potentially increasing needlestick injury risk. Affected lots were distributed nationwide with expiration dates through late 2025.
Ascend Laboratories LLC is recalling Cefixime Capsules 400 mg nationwide due to failed impurities and degradation specifications. The affected lot is Lot 20140282 with an expiration date of December 2021.
Sun Pharmaceutical is recalling Tadalafil Tablets USP 20 mg due to use of an incorrect grade of Crospovidone during manufacturing. The recall affects 36,786 bottles distributed to one distributor.
NOW Health Group Inc. is recalling NOW Ginseng & Royal Jelly 90 VCAPS and MMA Nutrition Ginselin 90 Veg Capsules because the products may contain Metronidazole, an undeclared pharmaceutical ingredient.
NOW Health Group Inc. is recalling NOW Royal Jelly 1500mg capsules and related private label versions because they may contain Metronidazole, an undeclared pharmaceutical ingredient. The recall affects approximately 88,890 units distributed across the United States and internationally.
NOW Health Group Inc. is recalling NOW Bee Pollen 500mg 100 VCAPS (UPC 733739025203) because the product may contain Metronidazole, an antibiotic not listed on the label.
Sun Pharmaceutical Industries is recalling Tadalafil 5 mg tablets (Lot # DNC1127A) because an incorrect grade of Crospovidone was used during manufacturing. The product was distributed to one distributor who may have further distributed it nationwide.
Precision Dose Inc. is recalling Acetaminophen Oral Suspension (325 mg/10.15 mL) due to contaminated raw ingredient used in manufacturing. The recall affects 151,100 unit dose cups distributed nationwide for hospital use.