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.
Gadget Island, Inc. is recalling Rhino 7 Platinum 5000 capsules because they contain undeclared active pharmaceutical ingredients and were marketed without FDA approval.
Health Matters America Inc. is recalling Organic Traditions Dark Chocolate Hazelnuts with Chili due to undeclared milk (casein). The product was distributed in 22 states and D.C.
Gadget Island, Inc. is recalling Grande X 5800 capsules because they contain undeclared prescription drugs sildenafil, desmethyl carbodenafil, and tadalafil.
Gadget Island, Inc. is recalling FIFTY SHADES 6000 capsules because they contain undeclared active pharmaceutical ingredients sildenafil, desmethyl carbodenafil, and tadalafil.
Forest River is recalling 2016-2018 Berkshire XLT motorhomes because incorrect circuit breakers may cause excessive heat and increase the risk of a fire.
Hyundai is recalling 2018 Santa Fe Sport vehicles because a side curtain air bag component may detach during deployment, increasing injury risk.
Health Matters America Inc. is recalling Organic Traditions Dark Chocolate Hazelnuts because they contain undeclared milk (casein). The products were distributed in 22 states and the District of Columbia.
East Manufacturing is recalling 2016-2018 Frame Dump trailers because cracks in the cross member may cause failure, increasing crash risk.
Honda is recalling specific 2010, 2016, and 2017 VT1300CX Fury motorcycles because missing welds on the fuel tank mounting bracket could cause fuel leaks and fire.
Health Matters America Inc. is recalling Organic Traditions Dark Chocolate Almonds because the product contains undeclared milk (casein).
Won Industry Co. is recalling three unapproved Compressible Limb Therapy Systems because they have incorrect air compression level setups. The devices were distributed in Maryland, Texas, and Mexico.
Becton Dickinson is recalling Trypticase Soy Agar with 5% Sheep Blood plates because they are contaminated with Listeria monocytogenes. The affected lots are distributed worldwide.
Biosense Webster is recalling 185 SMARTABLATE RF System Generators because they may inadvertently deliver RF energy if the foot pedal is placed near Stereotaxis magnets.
Becton Dickinson is recalling 2,598,000 BD Precision Glide Needles due to hub damage that can cause breakage or leakage during use.
Pro-Med Instruments is recalling DORO Sterile Disposable Skull Pins because two instances of pin tip breakage were reported during surgery.
Roche Diabetes Care is recalling the Accu-Chek Connect app because a bug in the Bolus Advisor feature may prevent correction bolus advice from being available for recent glucose readings.
Meijer Distribution is recalling specific lots of cashews that contain undeclared mixed nuts instead of chocolate covered cashews.
ICU Medical Inc is recalling MedNet 6.1 and 6.21 software because it may alter piggyback medication settings without user notice.
Biosense Webster is recalling PENTARAY NAV High-Density Mapping Catheters because the instructions for use were updated to indicate they should not be used in patients with prosthetic valves.
The Kroger Co. is recalling Comforts FOR BABY Purified Water with Fluoride Added after a complaint of mold was found in the product.
DeRoyal is recalling sterile custom surgical kits containing Medline Aplicare Povidone Iodine Prep Pads due to incorrect expiration dates.
Novo Nordisk is recalling specific batches of Dial-A-Dose insulin pen cartridge holders because they may crack or break when exposed to certain cleaning agents.
Won Industry Co. is recalling two Morning Life air compression devices because they were distributed without FDA approval and have incorrect air compression settings.
Fukuda Denshi is recalling DS-8100M and DS-8100N patient monitors because a damaged lithium-ion capacitor may cause a short-term battery error message.
Biosense Webster is recalling 73,796 PENTARAY NAV High-Density Mapping Catheters to update contraindication language in the Instructions For Use regarding prosthetic valves.