State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Strategic Sports is recalling specific Leather Up XElement motorcycle helmets that may not adequately protect users in a crash, failing federal safety standards.
Gamewell-FCI is recalling approximately 1,000 fire alarm panels because specific configurations may cause the system to fail to detect and respond to fire, smoke, or carbon monoxide alarms.
Creating X is recalling about 5,400 children's footed pajamas because they fail to meet federal flammability standards, posing a risk of burn injuries.
Nissan is recalling 2016 Frontier V6 vehicles because an incorrectly positioned starter wire harness may cause an electrical short and fire.
The Manhattan Toy Company is recalling Busy Loops table top toys because plastic beads can break off, posing a choking hazard. No injuries have been reported.
Grosfillex is recalling Havana commercial side chairs and armless bar stools because the backrest can crack and detach, posing a fall hazard.
CE North America is expanding a recall of KUL fan heaters sold at H-E-B in Texas due to a fire hazard. One overheating incident was reported, with no injuries or property damage.
Lipari Foods is recalling dark chocolate covered coffee beans due to an undeclared tree nut allergen (almonds). The product was distributed in eight states.
Siemens Healthcare Diagnostics is recalling IMMULITE 1000 Estradiol Test kits because the drug Faslodex may cause falsely elevated results.
Sagent Pharmaceuticals is recalling specific lots of Fluconazole Injection due to cross-contamination with metronidazole. The affected product is distributed nationwide and in Puerto Rico.
The FDA is recalling specific lots of Aplicare Castile Soap towelettes found in medical kits due to bacterial contamination.
Nestle is recalling Lean Cuisine Spinach Artichoke Ravioli due to the potential presence of glass pieces. Consumers should stop eating the product and return it to the store.
Covidien LLC is recalling Castile soap towelettes found in Foley trays and specimen kits because they are contaminated with bacteria.
Forest River is recalling 2008-2016 Puma recreational trailers and toy haulers because tires may contact the wheel well, risking deflation and loss of control.
Black Diamond is recalling 1.16 million climbing carabiners because they may unexpectedly open, posing a risk of injury or death from a fall.
FDA is recalling Aplicare Castile Soap towelettes in Foley trays and specimen kits due to bacterial contamination.
Nestle is recalling Lean Cuisine Marketplace Ricotta Cheese & Spinach Ravioli due to the potential presence of glass pieces.
Nestle is recalling Lean Cuisine Craveables Deep Dish Spinach & Mushroom pizza due to the potential presence of glass pieces.
FDA is recalling Castile soap towelettes in Foley trays and specimen kits due to bacterial contamination.
FDA is recalling Aplicare Castile Soap towelettes found in Foley trays and specimen kits due to bacterial contamination.
The FDA is recalling Castile soap towelettes included in Foley trays and specimen kits due to bacterial contamination.
FDA is recalling Castile soap towelettes used in Foley trays and specimen kits due to bacterial contamination.
Nestle is recalling specific DiGiorno, Lean Cuisine, and Stouffer's products due to the potential presence of glass pieces.
Aplicare Castile Soap towelettes found in Foley trays and specimen kits are being recalled because they are contaminated with bacteria.
Aplicare Castile Soap towelettes included in Foley Trays and Mid stream specimen kits are being recalled because they are contaminated with bacteria.