State
73,598 recalls have nationwide distribution and so reach Indiana. 9,592 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,592 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 2,534 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,592 recalls whose distribution notice names Indiana specifically. The 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Proterra is recalling 2019-2020 Catalyst buses because a power steering hose may leak fluid, increasing the risk of a crash.
Riverpoint Medical is recalling 1,276 units of Velosorb Fast Braided Absorbable Sutures because the product is non-sterile. This condition could compromise the sterile field and increase the risk of surgical site infection.
Riverpoint Medical is recalling 1,248 units of non-sterile Velosorb sutures due to a risk of surgical site infection.
FDA is recalling Endo GIA Auto Suture Universal Articulating Loading Units because staples may not form properly, potentially preventing adequate hemostasis during surgery.
Riverpoint Medical is recalling non-sterile Velosorb sutures that could increase the risk of surgical site infections.
Prestone is recalling about 687,000 antifreeze bottles because their caps may not engage the child-resistant mechanism, posing a poisoning risk to young children.
Riverpoint Medical is recalling 1,258 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.
Riverpoint Medical is recalling 3,110 units of non-sterile Velosorb sutures because they may compromise the sterile field and increase infection risk.
Riverpoint Medical is recalling non-sterile Velosorb Fast Braided Absorbable Sutures because they may compromise the sterile field and increase the risk of surgical site infection.
Riverpoint Medical is recalling 7,982 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.
Zeus Scientific is recalling 74 units of the ZEUS ELISA Parvovirus B19 IgM Test System due to false positive results identified during an FDA inspection.
Ameditech is recalling ProScreen Drugs of Abuse Tests because immunoassay enzymes failed performance standards, causing inconsistent detection of compounds.
Riverpoint Medical is recalling 1,267 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile. The defect could compromise the sterile field and increase the risk of surgical site infections.
Riverpoint Medical is recalling 1,244 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.
Riverpoint Medical is recalling 1,242 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.
Certain 2018-2021 Lance travel trailers are being recalled due to potential gas leaks in Dometic propane stoves that increase fire risk. Free repairs are available.
Riverpoint Medical is recalling 1,270 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.
Ameditech is recalling ImmuTest Drugs of Abuse Cups because they failed to consistently detect all compounds at labeled levels.
Encore Medical is recalling 37 humeral socket inserts because the size etched on the product may differ from the size on the patient sticker label.
Ameditech Inc is recalling 537,120 units of First Check 4 Panel Drug Cups because they may fail to consistently detect all compounds at labeled levels.
Olympus is recalling BF-Q180 bronchovideoscopes because they lack 510(k) clearance and are associated with a higher rate of patient infections.
Ameditech Inc is recalling 23,000 MicroScreen immunoassay units because they failed to consistently detect compounds at labeled levels.
Eagle Family Foods Group is recalling 365 Everyday Value Organic Classic Salted Popcorn because pieces of glass may be present in the product.
Office Depot is recalling 25,360 JINYINSHAN KN95 masks because test results showed they failed to filter more than 95% of particulates.
Encore Medical is recalling 15 units of RSP Standard Humeral Socket Inserts due to size labeling discrepancies that could lead to incorrect implantation.