State
73,806 recalls have nationwide distribution and so reach Indiana. 9,598 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,598 recalls naming Indiana we have scored against our rubric, 1,908 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,536 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,598 recalls whose distribution notice names Indiana specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Promise Pharmacy is recalling 139 vials of Ipamorelin and Sermorelin injections nationwide due to a lack of sterility assurance.
Promise Pharmacy, LLC is recalling 704 vials of Methylcobalamin 10,000 mcg Injection due to a lack of sterility assurance. The product was distributed nationwide in the USA.
Oskri Corp. is recalling Organic Peanut Spicy Cayenne Butter due to potential Listeria monocytogenes contamination. The recall was expanded to include all Oskri manufactured butters.
Promise Pharmacy is recalling 416 vials of Ipamorelin 9 mg injection because the product lacks sterility assurance. The affected lots were distributed nationwide.
Promise Pharmacy is recalling 5 vials of Myer's Cocktail due to a lack of sterility assurance. The product was distributed nationwide.
Promise Pharmacy, LLC is recalling 59 vials of IGF-1-LR3, 3 mg injection due to a lack of sterility assurance. The product was distributed nationwide in the USA.
Promise Pharmacy is recalling compounded Prednisolone and Gatifloxacin ophthalmic solution due to a lack of sterility assurance.
Dr. Reddy's Laboratories is recalling Levetiracetam Injection bags because the primary label incorrectly identifies the product strength and sodium chloride concentration.
Promise Pharmacy is recalling 55 bottles of compounded Prednisolone and Gatifloxacin Ophthalmic Solution due to a lack of sterility assurance.
Tris Pharma is recalling 35,280 bottles of Infants' Ibuprofen due to potential higher-than-labeled ibuprofen concentrations.
Tris Pharma is recalling specific lots of Infants' Ibuprofen because the medication may contain a higher concentration of ibuprofen than labeled.
Promise Pharmacy, LLC is recalling Folic Acid Injection, 10 mg/mL, 10mL vials due to a lack of sterility assurance. The affected lots were distributed nationwide.
Steris Corporation is recalling 129 ATLAS Loading Cars because the latch may fail to engage when empty, causing the unit to slide or fall.
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.