State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Michael's Naturopathic Programs is recalling Cholesterol Metabolism Factors tablets because they may contain undeclared milk and soy.
Chrysler is recalling 2016 Chrysler 200 vehicles because chassis fastener joints may not be tightened correctly, which could loosen and reduce steering capability.
Chrysler is recalling 2014-2016 Jeep Cherokee vehicles because seat fasteners may not be tightened correctly, increasing injury risk in a crash.
Let's Talk Health is recalling 417 bottles of Oxygen Nasal Wash because the product was marketed without FDA approval and does not comply with nasal decongestant monograph requirements.
Creative Snacks Co. is recalling specific lots of roasted, salted sunflower seeds due to the potential presence of Listeria monocytogenes.
Dennis East International is recalling whiskey glass and stone sets because the glass can break during use, posing a laceration risk.
Merge Healthcare is recalling 37 units of Merge HEMO software because the displayed International Normalized Ratio (INR) value does not match the imported value.
S-L Snacks NC, LLC is recalling Lance Oyster Crackers because they may contain low levels of peanut residue.
The Kroger Co is recalling Kroger Deluxe Ice Cream S'mores because it may contain undeclared peanut residue. The product was distributed to 29 states.
Philips is recalling UroDiagnost x-ray systems because bolts may break, causing the c-arm to move and sag.
Philips is recalling 993 MultiDiagnost Eleva x-ray systems because bolts attaching the clamping plate may break, causing the C-arm to sag.
Shocker Paintball is recalling RSX markers with blue main chambers because the part can unexpectedly eject from the rear, posing a risk of impact injury.
Stryker Medical is voluntarily recalling Spirit Plus hospital beds because broken actuators may cause the bed to lower unexpectedly, risking patient injury.
Philips is recalling 993 MultiDiagnost Eleva x-ray systems because bolts may break, causing the C-arm to sag. The recall covers units distributed worldwide.
Philips is recalling IntelliVue Patient Monitors because they may display outdated waveform data if powered on continuously for several months, failing to reflect current patient conditions.
Stryker Medical is voluntarily recalling Spirit Select and Spirit Plus hospital beds because broken actuators may cause the bed to lower unexpectedly, risking patient injury.
Isomeric Pharmacy Solution is recalling Betamethasone Acetate / Betamethasone Sodium Phosphate Injectable Suspension due to potential drug clumps and larger particle sizes.
Beckman Coulter is recalling AU480 Chemistry Analyzers because leaking C cups can cause coolant to short-circuit the instrument's circuit boards.
Beckman Coulter is recalling AU5800 Chemistry Analyzers because cracked C cups can leak coolant onto circuit boards, causing short-circuits and instrument stop mode.
Zimmer Surgical Inc is recalling 90 units of the Air Dermatome II Width Plate because the surface coating is blistering, peeling, and discoloring after use.
Merge Healthcare is recalling Merge PACS 6.0 software because it fails to display annotations on certain loaded studies.
Zimmer Surgical Inc is recalling 70 units of Air Dermatome II Width Plates because the surface coating is blistering, peeling, and discoloring after use.
Zimmer Surgical Inc is recalling 220 Air Dermatome II handpieces because the surface coating is blistering, peeling, and discoloring after use.
Medtronic Navigation is voluntarily recalling 27 units of StealthStation software due to compatibility issues with specific floor-based scanners.
Medtronic Navigation is conducting a voluntary field action for Synergy Cranial S7 software applications due to compatibility issues with specific floor-based scanners.