State
73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Chengdu Ai Qin E-commerce Co., Ltd. is recalling TTDEYE Devil Red colored contact lenses because they were distributed without FDA clearance.
Teleflex Medical Inc. is recalling 7,401 Rusch Greenlite laryngoscopes because the welded joint may break during use.
Teleflex Medical is recalling Rusch Greenlite laryngoscopes because the welded joints may break. The devices are used for tracheal intubation.
Medline Industries is recalling 2,440 units of ClearPro T-Piece Closed Suction Catheters because reports indicate the catheter may come apart from the device assembly during use.
Giant Eagle is recalling Dried Island Fruit Mix because it may contain undeclared peanut, almond, milk, and soy allergens.
Shanghai United Imaging Healthcare is recalling four uCT 530 Computed Tomography X-ray Systems because uneven metal edge overlap may create a sharp edge.
Teleflex Medical Inc is recalling Rusch Greenlite laryngoscopes because the welded joint may break. The recall covers 27,341 units distributed nationwide.
Hercules is recalling Moravian Star lights because they lack adequate wire size and overcurrent protection, posing fire and electrical shock risks.
Shanghai United Imaging Healthcare is recalling three uCT 550 Computed Tomography X-ray Systems because uneven metal edges on the mylar strip may create sharp edges.
Abbott is recalling Alinity ci System Control Modules because quality control results were not properly evaluated for failures.
Shanghai United Imaging Healthcare is recalling five uCT 760 CT systems because uneven metal edges on the mylar strip may create sharp edges.
Chengdu Ai Qin E-commerce Co., Ltd is recalling TTDEYE Radial Pink colored contact lenses because they were distributed without FDA clearance.
Teleflex Medical Inc. is recalling 29,740 Rusch Greenlite laryngoscopes because the welded joint may break. The devices are used for tracheal intubation.
Chengdu Ai Qin E-commerce Co., Ltd is recalling TTDEYE Flower Brown colored contact lenses because they were distributed without FDA clearance.
Built Brands LLC is recalling 242,400 peanut butter chocolate protein bars because they may be moldy before the expiration date.
MasterPharm LLC is recalling Tadalafil 3 mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling Progesterone Modified Release 200 mg Capsules because the company lacks processing controls to ensure the product meets specifications.
Built Brands LLC is recalling Cashew Caramel with Coconut Chocolate covered protein bars because they may be moldy before the expiration date.
Built Brands LLC is recalling S'Mores Chocolate covered protein bars because they may be moldy before the expiration date.
MasterPharm LLC is recalling Tadalafil 12 mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
Built Brands LLC is recalling Toffee Almond Chocolate covered protein bars because they may be moldy before the expiration date.
MasterPharm LLC is recalling Progesterone 300 mg Troches because the product lacks assurance of conformity to specifications.
Chengdu Ai Qin E-commerce Co., Ltd is recalling TTDEYE Diamonds Starlight colored contact lenses because they were distributed without FDA clearance.
MasterPharm LLC is recalling specific lots of Progesterone 200 mg Troches nationwide due to a lack of processing controls that ensures conformity to specifications.
Built Brands LLC is recalling Double Chocolate Mousse protein bars because they may be moldy before the expiration date. The recall covers 48,480 bars distributed in the U.S. and Canada.