State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Volkswagen is recalling 2012-2014 Passat diesel vehicles because a short heat shield may allow grease to leak and contact hot exhaust parts, increasing fire risk.
Daimler Trucks North America is recalling 2013-2018 Thomas Built Saf-T-Liner HDX school buses because seat lap belts may be anchored to the seat rather than the bus structure.
Meridian Medical Technologies is recalling EpiPen auto-injectors because the delivery system may fail to activate, preventing patients from receiving epinephrine.
Meridian Medical Technologies is recalling EpiPen Jr. auto-injectors because the delivery system may fail to activate, preventing patients from receiving epinephrine.
Olympus is recalling 863 Endoeye HD II video telescopes because a damaged temperature sensor can cause the tip to become abnormally hot.
Temsa is recalling 2014-2017 TS45 motorcoaches because improper fasteners on the leveling valve linkage may loosen and detach, potentially damaging tires and increasing crash risk.
Medtronic is voluntarily recalling Newport HT70 and HT70 Plus ventilators because they may shut down spontaneously without an alarm during normal operation.
Sysmex America Inc is recalling XN-10 and XN-11 hematology analyzers due to a risk of fire caused by misaligned internal protective sheets.
Roche Diabetes Care is recalling specific versions of the Accu-Chek Connect app because a bug in the Bolus Advisor feature may provide incorrect insulin dosing advice.
Natus Medical is recalling neoBLUE 2 phototherapy lights sold from 2003 to 2008 to prevent the use of replacement boards that allow higher light intensity than originally cleared.
Sprague Devices is recalling Heavy-Duty Bus Pantograph Wiper Arms because the mounting casting may crack, causing the arms to bend or detach and reducing driver visibility.
Dale Medical Products is recalling Stabilock Endotracheal Adhesive Bases because the adhesive faceplate may lose its properties and fail to adhere to the patient's face.
Breg Inc is recalling 2,609 units of Dressing Rect L (P/N 02428) because some may have unsealed pouches, rendering them non-sterile.
Graco is recalling specific My Ride 65 convertible child seats because the webbing may not adequately restrain a child in a crash, increasing injury risk.
Weaver Popcorn Co. is recalling Trail's End Chicago sports collection snack tins due to potential Salmonella contamination.
Bard Peripheral Vascular Inc. is recalling 570 units of MR GHIATAS Beaded Breast Localization Wire because they may be non-MR compatible instead of MR compatible.
AM Conservation Group is recalling about 37,000 luminescent night lights because they can overheat and pose a fire hazard. Consumers should stop using the products and contact the firm for a free replacement.
Roho Inc. is recalling 5,646 units of ROHO High and Mid Profile cushions because the Smart Check tool may cause improper inflation, increasing the risk of skin or soft tissue injury.
Breg Inc is recalling sterile dressings (P/N 02328) because a small percentage may have unsealed pouches, rendering them non-sterile.
Dale Medical Products is recalling Stabilock Endotracheal Tube Holders because the adhesive faceplate may lose its properties and fail to adhere to the patient's face.
The Anspach Effort, Inc. is recalling 182 Bearing Sleeve, 10CM Curved units because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 320 SC2100 Foot Controls because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 297 pneumatic system attachments because the supplied directions for use did not include a recommended service interval.
The Anspach Effort, Inc. is recalling 238 units of the 14cm QD Angle Attachment because the supplied directions for use did not contain a recommended service interval.
Smith & Nephew is recalling Renovation Thin Osteotome Blades because stability data does not support the labeled 10-year shelf life.