State
73,388 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 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
HD Premier is recalling DigitDots 3mm and 5mm magnetic balls because swallowed magnets can lodge in the digestive system, causing perforation, blockage, infection, and potentially death. Four children have required surgery to remove ingested DigitDots.
FXswede AB is recalling about 5,000 ToolGuards Portable Water Immersion Heaters sold on Amazon.com because the units can overheat, melt, or catch fire, creating electrocution and fire hazards. The firm has received 19 reports of overheating or fires and 2 reports of consumer shock.
Newmar is recalling 1,277 of its 2021 and 2022 motorhomes because the steering column bolt may not be properly tightened, potentially causing loss of steering control. Owners should contact dealers for free inspection and tightening.
Navistar is recalling 2018-2023 International LT vehicles with 1500W Purkeys inverter systems. The positive battery cable may be incorrectly routed, causing it to chafe and become damaged, which increases the risk of electrical fire.
General Motors is recalling 2014-2015 Chevrolet Equinox and GMC Terrain vehicles because corroded ball joints may cause windshield wipers to fail, reducing visibility.
Acme United is recalling PhysiciansCare brand over-the-counter pain relievers and aspirin because the packaging is not child-resistant as required by law, creating a poisoning risk for young children.
Abbott Similac For Spit Up Infant Formula with Iron is recalled due to consumer complaints of Cronobacter sakazakii and Salmonella Newport, with evidence of Cronobacter sakazakii found in the manufacturing facility.
Abbott Similac Pro-Sensitive Infant Formula is being recalled due to consumer complaints of Cronobacter sakazakii and Salmonella Newport in infants, with evidence of Cronobacter found in the manufacturing facility.
Abbott Similac Pro-Total Comfort Infant Formula is being recalled due to potential contamination with Cronobacter sakazakii and Salmonella Newport. Consumer complaints have been linked to these dangerous pathogens in affected infants.
Abbott is recalling Similac Alimentum infant formula due to consumer complaints of Cronobacter sakazakii and Salmonella Newport contamination, with evidence of Cronobacter in the manufacturing facility. The recall affects 40,943 cases.
Abbott Similac Alimentum Toddler Drink is recalled for consumer complaints related to Cronobacter sakazakii or Salmonella Newport contamination in infants, with Cronobacter sakazakii evidence found in the manufacturing facility.
Abbott is recalling Similac Sensitive Infant Formula with Iron due to potential Cronobacter sakazakii and Salmonella Newport contamination linked to consumer complaints about infant illness. The FDA classified this as a Class I recall.
Abbott Similac Organic infant formula products are recalled by the FDA due to potential Cronobacter sakazakii or Salmonella Newport contamination. Consumer complaints of illness in infants and manufacturing facility contamination triggered this Class I recall.
Abbott is recalling Similac For Spit Up Infant Formula due to contamination risks. Consumer complaints linked the product to Cronobacter sakazakii and Salmonella Newport, and Cronobacter was found in the manufacturing facility.
Abbott recalls Similac Advance Step-1 infant formula due to Cronobacter sakazakii and Salmonella Newport detected in the product and manufacturing facility, following consumer complaints in infants.
Abbott Similac Pro-Advance infant formula is being recalled due to potential contamination with Cronobacter sakazakii and Salmonella Newport. The FDA Class I recall affects products distributed nationwide and worldwide.
Abbott is recalling Similac infant formula products for possible contamination with Cronobacter sakazakii and Salmonella Newport following consumer complaints of illness in infants.
Abbott Similac PM 60/40 Low Iron Infant Formula has been recalled due to contamination with Cronobacter sakazakii and Salmonella Newport. The recall affects 8,358 cases distributed nationally and worldwide.
Abbott is recalling EleCare Junior Vanilla infant formula due to possible contamination with Cronobacter sakazakii or Salmonella Newport. The company found evidence of Cronobacter in the manufacturing facility and received consumer complaints.
Abbott Laboratories is recalling 22,074 cases of Similac for Supplementation infant formula due to potential Cronobacter sakazakii and Salmonella Newport contamination identified through consumer complaints and manufacturing facility testing.
Abbott is recalling EleCare Jr infant nutrition powder (203,416 cases) due to consumer complaints of Cronobacter sakazakii and Salmonella Newport in infants and contamination found in the manufacturing facility.
Abbott Laboratories is recalling Alimentum infant formula due to Cronobacter sakazakii detected in the manufacturing facility and consumer complaints of Cronobacter and Salmonella Newport in infants.
Custom Wheel House LLC is recalling specific Method Race Wheels because the spokes may crack under heavy loads, potentially causing a loss of vehicle control.
Abbott Laboratories is recalling EleCare infant formula nationwide and worldwide due to potential contamination with Cronobacter sakazakii and Salmonella Newport. Consumer complaints related to these pathogens have been received involving infants.
Abbott Similac Total Comfort Infant Formula with Iron is being recalled due to consumer complaints related to Cronobacter sakazakii and Salmonella Newport. The FDA classified this Class I recall affecting over 1.2 million cases.