State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Piazza Produce, Inc. is recalling specific Lemon Pepper products because the labels do not list ingredients, including undeclared soybean oil.
Natus Manufacturing Limited is recalling 31 Warmette Blanket and Dual Cabinets because a fuse may blow, causing power loss and potential melting of the fuse cover.
Piazza Produce, Inc. is recalling Salt Free Vegetable Herb products because the labels do not list ingredients, including undeclared soybean oil.
Piazza Produce, Inc. is recalling Quebec Chicken seasoning in various sizes because the product labeling does not list ingredients and contains undeclared soybean oil.
Piazza Produce, Inc. is recalling Jamaican Jerk seasoning in various sizes because the product labeling does not list ingredients, including undeclared soybean oil.
Forest River is recalling 2017 Prime Time Avenger recreational vehicles because incorrect Federal Placards may lead to tire over-inflation and blowouts.
Advanced Sterilization Products is recalling 107 EVOTECH Endoscope Cleaner and Reprocessor Systems because a hose may come loose and cause a leak.
Merge Healthcare is recalling Merge Eye Station software versions 11.6.0 and prior due to a risk of accidental patient record deletion.
Siemens Medical Solutions is recalling Biograph mCT Flow 40-4R scanners because laser cover windows may fall off.
Piazza Produce, Inc. is recalling three sizes of Cajun seasoning because the product labels do not list ingredients. The recall affects food service establishments in five states.
Straumann Manufacturing is recalling 165 dental implant drills because they cannot be inserted into handpieces due to tolerance specification failures.
Siemens is recalling IMMULITE 2000 Intact PTH assay kits because they may show a negative bias of up to -39% at low concentrations.
GE Healthcare is recalling OEC 9900 Elite and other mobile fluoroscopy systems because the workstation power cable assembly can fail intermittently.
Siemens Medical Solutions is recalling one Biograph mCT Flow Edge-4R scanner because laser cover windows may fall off.
Siemens Medical Solutions is recalling Biograph mCT-X scanners because laser cover windows may fall off.
Piazza Produce is recalling Herb De Provence in three sizes because the product labels do not list ingredients. The recall affects food service establishments in five states.
Piazza Produce, Inc. is recalling two sizes of curry powder because the product labeling does not contain a listing of ingredients.
Siemens Medical Solutions is recalling 88 Biograph mCT scanners because laser cover windows may fall off.
Straumann Manufacturing is recalling 120 units of Twist Drill PRO dental implant accessories because they cannot be inserted into handpieces due to tolerance specification failures.
Trilliant Surgical Ltd. is recalling Tiger Screw Sterilization Tray Base Assemblies due to a printing error on k-wire description markings.
Siemens is recalling 34 Biograph mCT scanners because laser cover windows may fall off, posing a potential hazard to users.
Bard Access Systems is recalling StatLock PICC Plus Crescent Foam devices because some pouches lack unique product identifiers like lot numbers.
GE Healthcare is conducting a voluntary field action for OEC MiniView 6800, OEC 9900 Elite, and OEC 9800 devices due to intermittent power cord failures.
Bard Access Systems is voluntarily recalling StatLock CV Plus catheter stabilization devices because some pouches lack unique product identifiers.
Siemens is recalling Artis zee/zeego angiographic x-ray systems due to potential high-voltage generator failures and rare image display loss.