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.
Asher's Chocolate Co. is recalling Milk Chocolate Cashew Praline bars due to potential Salmonella contamination. Consumers should stop eating the product and return it to the store.
Asher's Chocolate Co. is recalling specific lots of peanut butter cups due to potential Salmonella contamination. Consumers should check lot numbers and stop eating the product.
Asher's Chocolate Co. is recalling Dark Chocolate Molasses Pops due to potential Salmonella contamination. Consumers should stop eating the product and return it to the store.
Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.
Asher's Chocolate Co. is recalling specific lots of Milk Chocolate Cashew Praline due to potential Salmonella contamination.
Asher's Chocolate Co. is recalling specific lots of Milk Chocolate Candy Cups with M and M's due to potential Salmonella contamination.
Riser Holdings is recalling Chromag bicycle stems because clamping bolts may break, posing fall and injury hazards to riders.
Asher's Chocolate Co is recalling Peanut Butter Coated Mini Pretzels due to potential Salmonella contamination. Consumers should stop eating the product.
Asher's Chocolate Co is recalling White Confectionery Coating due to potential Salmonella contamination. Consumers should check their lot numbers and stop using the product.
Asher's Chocolate Co is recalling Dark Chocolate Almond Paw products due to potential Salmonella contamination. Consumers should check for Lot # 000336473.
Taro Pharmaceuticals is recalling Nystatin and Triamcinolone Acetonide Cream because it failed content uniformity specifications during 18-month stability testing.
Alcon is voluntarily removing 561,702 Patient Care Kits from the US market because the supplier reported potential sterile packaging compromise.
Smith & Nephew is recalling 100 units of D-RAD orthopedic screws because the expiration dates on the labels are incorrect and later than the actual expiration dates.
Verathon is recalling GVL 2 Stat blades (lot GC32825) because they were physically packaged with the incorrect size device, GVL 1 Stat blades.
Merge Healthcare is recalling Eye Station and Eye Care PACS software because antivirus programs may permanently delete newly captured medical images.
Smith & Nephew is recalling 197 units of D-RAD locking screws because the expiration dates on the labels are incorrect and later than the actual expiration dates.
Smith & Nephew is recalling 19 units of D-RAD locking pegs because the expiration dates on the labels are incorrect and later than the actual dates.
Smith & Nephew is recalling specific Peri-Loc VLP self-tapping cortex screws because the expiration dates printed on the labels are incorrect and later than the actual dates.
Ace Surgical Supply Co., Inc. is recalling 87 INFINITY Internal Hex Healing Abutments because the incorrect device was packaged.
Volkswagen Group of America is recalling 2,091 2015 Audi A3 Cabriolet vehicles because the safety certification label displays an incorrect production date.
Teleflex Medical is recalling Arrow EZ-IO Needle Sets because some individual unit pouches are missing lot numbers and expiration dates.
Valeant Pharmaceuticals is voluntarily recalling 5,647 units of CLENZIderm M.D. Acne Treatment Systems nationwide due to product discoloration.
Valeant Pharmaceuticals is voluntarily recalling CLENZIderm M.D. Pore Therapy Salicylic Acid 2% Acne Treatment due to discoloration.
Grand Design is recalling 2017-2018 Imagine travel trailers because slide room screws may shear, allowing the room to extend while towing and increasing crash risk.
Zutano is recalling about 38,000 infant Cozie booties because the rubber grips on the bottom can detach and pose a choking hazard.