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.
Meijer Distribution is recalling specific Ham & Cheddar on White Baguette Sandwiches due to potential Listeria monocytogenes contamination.
Meijer Distribution is recalling Colby and Colby Jack deli cheese due to potential Listeria monocytogenes contamination. The product was sold by weight in six states.
E-One is recalling 2013-2016 Quest, Typhoon, and Cyclone II emergency vehicles because front suspension ball joints can loosen and separate, potentially causing a loss of steering control.
Mylan Pharmaceuticals is recalling specific lots of Atorvastatin Calcium 10 mg tablets due to potential microbial contamination and elevated bioburden.
Merit Medical Systems is voluntarily recalling 1,265 units of 7F Prelude Short Sheath Introducers because the sheath marker tips may detach during use.
Mylan Pharmaceuticals is recalling Atorvastatin Calcium Tablets, 80 mg, due to potential microbial contamination and elevated bioburden.
Lipari Foods is recalling Old Tyme Firecracker Jack Mini Horn cheese due to potential Listeria monocytogenes contamination from a supplier.
Meijer Distribution is recalling 8oz packages of Artisan Made Natural Muenster Cheese due to potential Listeria monocytogenes contamination.
Lipari Foods is recalling Old Tyme Muenster Cheese due to potential Listeria monocytogenes contamination from a supplier.
Mylan Institutional, Inc. is recalling 1,527 cartons of Atorvastatin Calcium 10 mg tablets due to potential microbial contamination and elevated bioburden.
Stryker is recalling 292 Visum LED Surgical Lighting systems because missing screws and user overloading may cause the equipment to fall.
Tiffin is recalling 2017 Allegro Breeze motorhomes because front suspension ball joints can loosen, potentially causing a loss of steering control.
Claris Lifesciences Inc. is recalling Levofloxacin Injection due to a potential leak that may compromise sterility. The recall covers 24,456 units distributed nationwide.
Claris Lifesciences Inc. is recalling Ciprofloxacin in Dextrose Injection due to a potential leak that may compromise sterility.
Claris Lifesciences is recalling Fluconazole Injection due to a potential leak that could compromise sterility and contaminate the product.
Hospira is recalling 62,847 Plum 360 Infusion Pumps with software version 15.02 due to a defect that causes therapy to stop and incorrect alarms to display.
Merge Healthcare is recalling iConnect Enterprise Archive software because archived studies cannot be opened or sent to PACS, preventing physicians from reviewing comparison studies.
Merge Healthcare is recalling iConnect Enterprise Archive software versions that may fail to display prior medical images, potentially delaying treatment.
Meijer is recalling pre-made Caesar salads that were mislabeled as Greek salads and contain undeclared wheat. The affected products were distributed in six states.
Zimmer Biomet is recalling 141 units of the Altius M-INI OCT Posterior Spinal Fixation System because the driver cannot mate with the screw head tulip.
Bitterman and Sons is recalling Parmesan Truffle Salt because the label declares Parmigiano Reggiano cheese but fails to list milk as an ingredient.
Streck is recalling 128,692 Cyto-Chex BCT blood specimen collection tubes because the 2.0ml tube stoppers may come loose during phlebotomy if small diameter tube adapters are not used.
Strata Skin Sciences is recalling XTRAC Excimer Lasers because loose switch control wires may short, leading to unintentional laser firing.
Data Innovations, LLC is recalling JResultNet software because a defect may cause one patient's test results to be associated with another patient.
Hitachi Aloka Medical is recalling Prosound F75 ultrasound systems because the monitor arm may loosen. Affected units were distributed to specific US states.