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.
Medtronic Perfusion Systems is recalling DLP Pressure Monitoring Extension Line Adapters due to small pinholes in sterile packaging.
Channel Fish Processing Co. Inc. is recalling raw Oriental Breaded Fish Portions due to undeclared milk. The product was distributed to 14 states.
Channel Fish Processing Co. Inc. is recalling Channel Brand Raw Breaded Cod Tails due to undeclared milk. The product was distributed to 14 states.
Channel Fish Processing Co. Inc. is recalling Channel Brand Raw Breaded Haddock Cuts because the product contains undeclared milk, a major food allergen.
Channel Fish Processing Co. Inc. is recalling Channel Brand Raw Breaded Natural Flounder Fillets due to undeclared milk, a major food allergen.
Channel Fish Processing Co. Inc. is recalling Channel Brand Raw Breaded Pollock Squares due to undeclared milk. The product was distributed to 14 states.
Medtronic is recalling DLP Antegrade/Retrograde Adapters because small pinholes were found in a single packaging configuration of sterile pouches.
Channel Fish Processing Co. Inc. is recalling raw breaded whiting squares because the product contains milk, which is not declared on the label.
Channel Fish Processing Co. Inc. is recalling raw Oriental Breaded Fish Portions due to undeclared milk. The product was distributed to 14 states.
Medtronic Perfusion Systems is recalling DLP Pressure Disposable Pressure Display Sets because small pinholes were found in the sterile packaging.
Atrium Medical Corporation is recalling specific iCAST and Advanta V12 covered stents because the catheter hub was printed with incorrect dimensional information.
Medtronic Perfusion Systems is recalling DLP Cardioplegia Adapters with Pressure Port because small pinholes were identified in a single packaging configuration of sterile pouches.
Cardinal Health is recalling specific lots of sterile surgical drapes because the outer labels do not match the packaged product inside.
Cardinal Health is recalling specific lots of Tiburon Arthroscopy Drapes because the outer labels do not match the packaged product.
MixBin Electronics is recalling liquid glitter iPhone cases because the contents can leak and cause skin irritation or chemical burns.
Timken is recalling specific rear hub unit bearings for 2011-2017 Ford Explorer 4X2 vehicles because they lack a self-retention feature, which could cause the wheel to separate.
Utility Trailer is recalling 2017 VS2RA trailers because a weld defect may allow the mud flap bracket to detach, creating a road hazard.
Panelcraft is recalling Rainbow Dream Builder and Solid Builder sets because corner welds can break, releasing magnets that pose a choking hazard to children.
Carli Suspension is recalling adjustable track bars for specific Ram trucks because a joint may break, causing loss of steering and increasing crash risk.
Vantage Mobility International is recalling 2017 Chrysler Pacifica lowered floor vehicles because rear pinion brackets may crack, causing wheel wobble and potential loss of control.
Daimler Vans USA is recalling 2010-2011 Freightliner and Mercedes-Benz Sprinter 2500 and 3500 vehicles because passenger air bag inflators may rupture during deployment.
Dana is recalling Spicer D-Series and E-Series steer axles because the castellated nut may not be properly torqued, allowing the tie rod to loosen and potentially disconnect.
Daimler Vans USA is recalling 2012 Freightliner and Mercedes-Benz Sprinter 2500 and 3500 vehicles because the passenger air bag inflators may rupture during deployment, posing a risk of serious injury or death.
Nestlé Waters is recalling about 12,300 AccuPure floor-standing filtration dispensers because they can overheat, smoke, or catch fire. No injuries have been reported.
Daimler Vans USA is recalling 2007-2009 Dodge and Freightliner Sprinter 2500 and 3500 vehicles because passenger air bag inflators may rupture in a crash.