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.
Key Pharmacy and Compounding Center is recalling Vitamin D3 in Olive Oil SDV 100,000U/mL Injection due to a lack of assurance of sterility.
Mobius Medical Systems is recalling Mobius3D software versions 1.5.0 and 1.5.2 due to a code defect that may cause dose calculation discrepancies in radiation therapy.
Sumitomo is recalling specific Dunlop Sportmax Q3+ motorcycle tires due to air pockets in the shoulder that may affect handling and increase crash risk.
Key Pharmacy and Compounding Center is recalling specific lots of PGE1/Procaine injection because the firm cannot ensure the sterile compounded drugs are free from contamination.
Key Pharmacy and Compounding Center is recalling specific lots of Procaine HCL 1% injections because the firm cannot ensure the products are sterile.
Key Pharmacy and Compounding Center is recalling specific lots of Hydroxo-B12 injections because the firm cannot assure the sterility of the products.
Keystone is recalling 2012-2018 Springdale 303BH RVs because Federal Identification Tags overstate axle weight capacity, potentially leading to vehicle overload.
Molnlycke Health Care is recalling 956 units of the Brennen Skin Graft Mesher because of a sterilization validation failure. The instruments were distributed domestically and internationally.
Medline Industries is recalling 10 mm Distraction Pins because the sterile packaging seal may be compromised, potentially causing the device to lose sterility.
Williams-Sonoma is recalling Rejuvenation Cypress and Imbrie wall sconces because the articulating joint can pinch wires, creating a shock risk.
Herbalife is recalling Peanut Butter Protein Bars because they may contain trace amounts of fish gelatin, an undeclared allergen.
Armour Eckrich Meats is recalling approximately 90,978 pounds of ready-to-eat sausage products that may contain pieces of metal. No adverse reactions have been reported.
Taro Pharmaceuticals is recalling specific lots of Fluocinonide Cream 0.05% due to cross-contamination with hydrocortisone-17-valerate.
Zimmer CAS is voluntarily recalling 152 units of the Navitrack System - OS Knee Universal due to software anomalies corrected in a new revision.
Medline Industries is recalling 2,112 packs of sterile distraction pins because the packaging seal may be compromised, risking loss of sterility.
Medline Industries is recalling 300 packs of 12 mm Distraction Pins because the sterile packaging seal may be compromised, potentially allowing the device to lose sterility.
Zimmer Biomet is recalling specific lots of NexGen Offset Stem Extension implants because the size etched on the parts and packaging was incorrect.
Zimmer CAS is voluntarily recalling Navitrack System OS Knee Universal software versions due to software issues causing errors and discrepancies.
Teleflex Medical is recalling Visistat 35R Disposable Skin Staplers because some boxes are mislabeled as containing Wide devices when they contain Regular devices.
Medical Action Industries is recalling specific lots of Blue OR Towels because lint was found on the sterile towels.
Medical Action Industries is recalling sterile operating room towels because lint is present on the product.
Medtest Holdings is recalling Pointe Scientific Hitachi AST Reagent because the package insert contains inconsistent linearity values in different sections.
Pier 1 Imports is recalling Temani wicker chairs, settees, and ottomans because the paint may contain excessive lead, violating federal standards.
Hobby Lobby is recalling Easter and July 4th-themed light-up spinner toys because the battery cover can detach, exposing coin cell batteries that pose choking and ingestion hazards to young children.
REV is recalling 24 Road Rescue emergency vehicles because short bolts may fail to secure the cot during a crash, potentially injuring occupants.