State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Halyard Health is recalling specific lots of saline vials used in closed suction systems because they may leak, potentially exposing the contents to infectious agents.
Halyard Health is recalling Turbo-Cleaning Closed Suction Systems because 15ml saline vials may leak, potentially exposing contents to infectious agents.
Medline Industries is recalling 190 units of pediatric elbow closed suction catheters because they were distributed before being sterilized.
GKI Foods is voluntarily recalling multiple Dark Chocolate Cranberry products because they may contain an undeclared milk allergen.
Exactech is recalling 893 Optetrak Offset Tibial Trays and Screws because of a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.
Halyard Health is recalling specific lots of saline vials used in closed suction systems because they may leak, potentially exposing contents to infectious agents.
Exactech is recalling 801 Optetrak Offset Tibial Trays and Screws due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.
GKI Foods is voluntarily recalling Dark Chocolate Powerberry products because they may contain an undeclared milk allergen.
Shoreline Fruit is voluntarily recalling dark chocolate covered cherries because the supplier recalled dark chocolate containing undeclared milk.
GKI Foods is voluntarily recalling Dark Chocolate Coffee Beans because they may contain an undeclared milk allergen.
GKI Foods is voluntarily recalling multiple Dark Chocolate Almond products because they may contain an undeclared milk allergen.
Halyard Health is recalling specific lots of Closed Suction Systems because the saline vials may leak, potentially exposing contents to infectious agents.
Libbey Glass is recalling approximately 229,000 Bourbon Taster Glasses because they can break during normal use, posing a laceration hazard.
GKI Foods is voluntarily recalling Dark Chocolate Blueberries because they may contain undeclared milk. Consumers with milk allergies should not eat the product.
Exactech, Inc. is recalling 840 Optetrak Constrained Condylar Offset Screws because of a design incompatibility with certain tibial inserts and trays.
GKI Foods is voluntarily recalling Dark Chocolate Pecans because they may contain an undeclared milk allergen.
Exactech, Inc. is recalling 114 Optetrak Offset Tibial Trays and Screws due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.
Medline Industries is recalling 1,428 plastic transfer belts because the locking mechanism may fail, allowing the strap to slip through the buckle.
Medline Industries is recalling 120 units of sterile suction catheters that were distributed before being sterilized.
Exactech is recalling 895 Optetrak Constrained Condylar Offset Screws because they are incompatible with certain tibial inserts and trays.
GKI Foods is voluntarily recalling Dark Chocolate Raisins because they may contain an undeclared milk allergen. The recall covers multiple lot sizes and distribution states.
GKI Foods is voluntarily recalling Dark Chocolate Ginger Snap Cookies because they may contain an undeclared milk allergen.
Zimmer Biomet is recalling 29 ROSA Surgical Devices due to a software issue affecting cooperative endoscopy mode.
Leading Pharma, LLC is recalling Lorazepam tablets labeled as 0.5 mg but containing 1 mg. The recall addresses a labeling error affecting 2,952 bottles nationwide.
West-Ward Pharmaceuticals is recalling specific lots of Dexamethasone Sodium Phosphate Injection because of high out-of-specification results for a related compound.