State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
West-Ward Pharmaceuticals is recalling Dexamethasone Sodium Phosphate Injection due to high levels of a related compound impurity.
Zero Motorcycles is recalling 36 units of 2018 motorcycles because the Vehicle Emission Control Information label may display the wrong model year.
Daimler Trucks North America is recalling 2008-2018 Freightliner and Western Star trucks because the brake light switch may fail to activate lights after hard braking, increasing crash risk.
Gulf Stream Coach is recalling 2018 Geo and Breeze trailers because the Federal label incorrectly lists two axles instead of one, failing certification requirements.
Meijer Distribution is voluntarily recalling mixed pepper blend and other vegetable products due to potential Listeria monocytogenes contamination from a supplier.
Meijer Distribution is voluntarily recalling specific cauliflower floret products due to potential Listeria monocytogenes contamination identified by a supplier.
Meijer is voluntarily recalling specific salad rotini products due to potential Listeria monocytogenes contamination from a supplier.
Meijer Inc. is voluntarily recalling multiple processed vegetable products, including Brussels sprouts slices, due to potential Listeria monocytogenes contamination.
Meijer Distribution is voluntarily recalling zucchini squash and other vegetable products due to potential Listeria monocytogenes contamination.
Meijer Distribution is voluntarily recalling processed vegetable products, including Zucchini and Squash Combo, due to potential Listeria monocytogenes contamination from a supplier.
Meijer Distribution is voluntarily recalling specific vegetable products, including a Fiesta Tray with Red Pepper Hummus, due to potential Listeria monocytogenes contamination.
Meijer is voluntarily recalling specific broccoli floret products due to potential Listeria monocytogenes contamination identified by a supplier.
doTERRA is voluntarily recalling Slim & Sassy TrimShake mixes because they contain an undeclared milk allergen.
Meijer is voluntarily recalling asparagus products due to potential Listeria monocytogenes contamination identified by a supplier.
Meijer is voluntarily recalling Large, Medium, and Small Veggie Trays due to potential Listeria monocytogenes contamination from a supplier.
Meijer is voluntarily recalling fresh vegetable trays with hummus due to potential Listeria monocytogenes contamination from a supplier.
doTERRA is voluntarily recalling Slim & Sassy TrimShake chocolate and vanilla mixes because they contain an undeclared milk allergen.
DRV Suites is recalling specific recreational vehicles equipped with certain Kidde fire extinguishers that may clog, require excessive force to activate, or have nozzles that detach.
WalkMed, LLC is recalling 25,920 infusion pump reservoir bags due to reported fluid leaks at the luer connection.
Aurora Products is recalling Dark Chocolate Cherries in 8.5 oz cups and 11 oz tubs due to undeclared milk.
Bison Coach is recalling 2010 Stratus, Aluma Sport, Trail Express, and Trail Hand trailers because their fire extinguishers may clog or detach, posing injury risks.
Zimmer Biomet is recalling 21 ROSA Surgical Devices due to a possible break in the Force Sensor connector. The devices were distributed to facilities in Ohio, Michigan, and Texas.
Meijer is voluntarily recalling dark chocolate coffee beans, almonds, and cashews due to undeclared milk.
Beckman Coulter is recalling 268 AQUIOS CL Flow Cytometers because the system may duplicate sample requests, leading to sample misidentification when connected to a Laboratory Information System.
Zimmer Biomet is recalling 53 ROSA Surgical Devices because of observed instability. The devices are computer-controlled arms used in neurosurgery.