State
73,718 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 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
SCA Pharmaceuticals is recalling 3,932 bags of Heparin Sodium 5,000 units due to out-of-specification potency results at the 30-day stability timepoint.
Keystone is recalling certain 2021 Outback travel trailers because the Federal Identification Tag incorrectly states tire pressure should be 65 PSI instead of the correct 80 PSI. Underinflated tires could fail and increase crash risk.
Ion Beam Applications is recalling four Proteus 235 Proton Therapy Systems because a software defect prevents users with long names from resuming interrupted treatments.
Eosera, Inc. is voluntarily recalling specific lots of Ear Itch MD sprays nationwide due to cGMP deviations.
Hasbro is recalling Super Soaker XP 20 and XP 30 water blasters because decorative stickers contain lead levels exceeding federal bans. No injuries have been reported.
Anjon Holdings is recalling 249 Anjon Bremer Molded Crown bone fixation fasteners because of a high rate of galling in a threaded component.
Eosera, Inc. is voluntarily recalling 43,424 bottles of Ear Itch MD Anti-Itch Spray due to cGMP deviations. The product was distributed nationwide in the United States.
Signature Hardware is recalling Bastian Teak medicine cabinets because the mirrors can detach and fall, posing an injury hazard. Consumers should contact the company for a free in-home repair.
Pier 1 Imports is recalling specific three-wick Halloween candles because high flames can ignite the wax, posing fire and burn risks.
Ortho Clinical Diagnostics is recalling VITROS Anti-SARS-CoV-2 Total Reagent because swapped bottles may cause false negative or delayed results.
Shanghai United Imaging Healthcare is recalling one uEXPLORER PET/CT Diagnostic Imaging System in Texas due to potential sharp edges and image data issues.
Smith & Nephew is recalling 1,845 tibial knee prostheses because raw material inconsistencies may cause internal non-homogenous material defects.
Shanghai United Imaging Healthcare is recalling four uMI 550 PET/CT systems due to defects that may cause image artifacts, scanning interruptions, or sharp edges.
Spartan Fire is recalling one 2018 Gladiator vehicle because its exterior LED lights may be too bright, potentially blinding other drivers and increasing crash risk.
Flower Orthopedics is recalling 25 calcaneus plates because the contract manufacturer used a titanium alloy instead of pure titanium.
Ortho Clinical Diagnostics is recalling VITROS Anti-SARS-CoV-2 IgG Reagent Packs because swapped reagent bottles may cause false negative or delayed results.
Lithonia Lighting is recalling CFMK Surface Mount Brackets because they can fail to secure CPANL LED fixtures, causing them to fall and pose an impact injury risk.
Luminex is recalling Verigene Processor SP systems because an instrument failure may cause false negative results in blood culture tests.
James Skinner Baking Co. is recalling Marketside Peanut Butter Brownies because units may lack the ingredient list, failing to declare major allergens including peanuts, wheat, milk, egg, and soy.
Indianapolis Fruit Company is recalling Garden Cut Organic Coleslaw w/ Carrots because pieces of plastic were found in the finished product.
Flower Orthopedics is recalling 25 calcaneus plates because they were manufactured with a titanium alloy instead of pure titanium.
Eosera, Inc. is voluntarily recalling 45,673 bottles of Ear Pain MD Pain Relief Drops For Kids due to cGMP deviations.
Flower Orthopedics is recalling 25 calcaneus plates because the manufacturer used a titanium alloy instead of pure titanium.
Pharmaceutical Associates, Inc. is recalling Nystatin Oral Suspension because it failed potency testing. Patients should consult their healthcare provider.
Hostess Brands is recalling 34,409 cases of Raspberry Zingers cakes nationwide due to potential mold growth prior to the best-by date.