State
73,738 recalls have nationwide distribution and so reach Indiana. 9,596 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,596 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 9,596 recalls whose distribution notice names Indiana specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Sun Organic is recalling Wintergreen Essential Oils because the packaging is not child-resistant, posing a poisoning risk to young children.
Honda is recalling 2020 Pilot and Passport vehicles because the certification label ink may wipe away, removing weight rating information and increasing crash risk.
Rooms To Go is recalling Patmos Chaise Lounge Chairs because the paint on the metal frame contains lead levels that exceed federal standards.
Rawlings is recalling approximately 1,400 CHMACH-SR Senior Catcher's Helmets because the back plate may fail to protect the player, posing a risk of head injury.
Freedman Seating Company is recalling certain seat assemblies because the seat belt retractor block out zone may not be set correctly, potentially failing to secure occupants.
Country Home Products is recalling specific DR walk-behind leaf blowers because internal blades can break off and discharge, posing a projectile hazard.
Mazda is recalling 2016 CX-5 vehicles because the LED Daytime Running Lights may fail, potentially reducing visibility and increasing crash risk.
Spartan Motors is recalling 2019 Utilimaster Sprinter vehicles because the rear camera display may fail, increasing the risk of a crash.
Juratoys is recalling Sophie la Giraffe Bead Maze toys because a wooden triangle piece poses a choking hazard to young children. No injuries have been reported.
Infantino is recalling about 14,000 infant carriers because the buckles can break, posing a fall hazard. No injuries have been reported.
Dianne's Fine Desserts is recalling frozen Sienna Chocolate Turtle Brownies because they contain undeclared peanuts. The product was distributed in Michigan, Illinois, and Indiana.
Radiometer Medical ApS is recalling AQURE basic system software versions 2.3.5 and below due to a potential patient data mix-up risk when connected to third-party devices.
Whole Foods Market is recalling 365 Everyday Value Dark Chocolate Peppermint Sandwich Cremes because they may contain undeclared milk.
Shandex Personal Care Manufacturing Inc. is recalling Walgreens Acne Cleansing Bar due to the presence of a visible metal contaminant.
Jeni's Splendid Ice Creams LLC is recalling 49,358 pints of Dairy Free Cold Brew with Coconut Cream frozen dessert because they may contain undeclared milk.
Tesla is recalling 2015-2016 Model X vehicles because aluminum steering bolts may corrode and fracture, causing loss of power steering assist.
Whole Foods Market is recalling 365 Everyday Value Dark Chocolate Caramel Sea Salt Sandwich Cremes due to potential undeclared milk and coconut.
Haemonetics is recalling specific Cell Saver bowl sets because they may leak, potentially trapping fluid and causing incomplete washing.
Haemonetics is recalling Cell Saver bowl sets because cracks in the inner core may cause leaks and incomplete blood washing.
LivaNova USA Inc is recalling 106 Cyberonics VNS Therapy AspireHC Model 105 generators due to electrical leakage causing premature battery depletion.
Haemonetics is recalling 739 Cell Saver bowl sets because cracks in the inner core can cause leaks and incomplete blood washing.
Haemonetics is recalling CS Elite Processing Sets because cracks in the bowl core may cause fluid trapping and incomplete washing.
Vitreq Bv is recalling VitreQ 23G Silicone Tipped Cannulas because microscopic tears in the sterile pouch may compromise sterility.
Vitreq Bv is recalling VitreQ 20G Blunt and Brush Needles because microscopic tears in the sterile pouch may compromise sterility.
Vitreq Bv is recalling VitreQ 23G VFI Cannulas because microscopic tears in the sterile pouch may compromise sterility.