State
73,741 recalls have nationwide distribution and so reach Alabama. 6,377 additional recalls listed Alabama specifically in their distribution scope.
Of the 6,377 recalls naming Alabama we have scored against our rubric, 1,129 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,604 (25%) are Severe.
Which agencies issued them
These figures cover only the 6,377 recalls whose distribution notice names Alabama specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Chicago Bar Company LLC is voluntarily recalling RXBAR Chocolate Chip bars due to undeclared peanut. Consumers should stop eating the product.
Chicago Bar Company is voluntarily recalling RXBAR Mixed Berry bars due to undeclared peanut. Consumers should stop eating the product and return it to the store.
AtriCure is recalling 1,288 COBRA FUSION 50 Ablation Systems because patients may face an elevated risk of thromboembolism during specific off-pump procedures.
Promise Pharmacy is recalling 59 vials of IGF-1 LR3 injections because they lack sterility assurance. The affected products were distributed nationwide.
Philips is recalling 146 CombiDiagnost R90 X-ray systems because a software defect may cause patients to receive increased radiation doses.
Chicago Bar Company LLC is voluntarily recalling RXBAR Pumpkin Spice bars due to undeclared peanut allergen.
RXBAR is voluntarily recalling Kids Chocolate Chip bars because they contain undeclared peanut, a major food allergen.
Chicago Bar Company LLC is voluntarily recalling RXBAR 12-Bar Variety Packs because they contain undeclared peanut, a major food allergen.
Porsche is recalling one 2019 Cayenne Turbo because shock absorber forks may allow the shock absorbers to loosen, potentially impairing steering.
Chicago Bar Company LLC is voluntarily recalling RXBAR KIDS Apple Cinnamon Raisin bars because they contain undeclared peanut.
Chicago Bar Company LLC is voluntarily recalling RXBAR Apple Cinnamon bars due to undeclared peanut. Consumers should check Best By dates and stop eating the product.
AtriCure is recalling 175 units of the COBRA FUSION 150 Ablation System because patients may face an elevated risk of thromboembolism during specific off-pump procedures.
Chicago Bar Company LLC is voluntarily recalling KIDS Berry Blast bars because they contain undeclared peanut, a major food allergen.
Promise Pharmacy, LLC is recalling 8 vials of Pyridoxine HCl Injection due to a lack of sterility assurance. The product was distributed nationwide in the USA.
Chicago Bar Company LLC is voluntarily recalling RXBAR 10-Bar Variety Packs because they contain undeclared peanut, a major food allergen.
Chicago Bar Company LLC is voluntarily recalling RXBAR Mint Chocolate bars due to an undeclared peanut allergen. The recall affects single, 4-count, and 12-count cartons.
Crate and Barrel is recalling Holiday Bear Acrylic Milk Bottles because the included plastic straw can crack or break, posing a laceration hazard.
Chicago Bar Company LLC is voluntarily recalling RXBAR Coffee Chocolate bars due to undeclared peanut. Consumers should check Best By dates and stop eating the product.
Chicago Bar Company LLC is voluntarily recalling Coconut Chocolate RXBARs because they contain undeclared peanut, a major food allergen.
Chicago Bar Company LLC is voluntarily recalling RXBAR 14-Bar Variety Packs because they contain undeclared peanut, a major food allergen.
PBM Nutritionals is recalling specific lots of Parent's Choice and Little Journey toddler milk drink powder because the product may contain foreign material.
Chicago Bar Company LLC is voluntarily recalling RXBAR variety packs because they contain undeclared peanut, a major food allergen.
Chicago Bar Company LLC is voluntarily recalling RXBAR Chocolate Hazelnut bars due to undeclared peanut. Consumers should stop eating these bars.
Porsche is recalling 14,110 vehicles because the instrument cluster may fail to warn drivers when brake pads are worn out, increasing crash risk.
Volkswagen is recalling 2019 Jetta vehicles because an incorrect driver frontal airbag may have been installed during a service visit, potentially increasing injury risk in a crash.