State
72,913 recalls have nationwide distribution and so reach Illinois. 11,602 additional recalls listed Illinois specifically in their distribution scope.
Of the 11,602 recalls naming Illinois we have scored against our rubric, 2,039 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,515 (22%) are Severe.
Which agencies issued them
These figures cover only the 11,602 recalls whose distribution notice names Illinois specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Albertsons store-made Meal Salmon Cajun is being recalled because the contains statement does not declare salmon. 40 units are affected.
Albertsons store-made Shrimp 16-20 Kabob Pollo Asada Marinade is being recalled because the contains statement does not declare shrimp. Four units are affected.
Albertsons store-made Salmon Fillet Pollo Asado Marinade is being recalled because the contains statement does not declare salmon. Two units are affected.
B. Braun CESK Northside Anesthesia Trays are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering it unusable.
Albertsons store-made Grain Bowl Salmon Quinoa Lentil is being recalled because the contains statement does not declare salmon. Nine units are affected.
Albertsons store-made Ready Meals Tuna Salad & Muenster Cheese Snack Pack is being recalled because the contains statement does not declare tuna. 237 units are affected.
Albertsons store-made Parmesan Crusted Tilapia is being recalled because the contains statement does not declare tilapia. 15 units are affected.
Albertsons store-made Chimichurri Shrimp Bowl is being recalled because the contains statement does not declare shrimp. 20 units are affected.
Xyvona levorphanol tartrate tablets, 3 mg, are being recalled following FDA's denial of marketing the product under the proprietary name Xyvona.
Albertsons store-made Ready Meals Sandwich Tuna Salad Croissant is being recalled because the contains statement does not declare tuna. 156 units are affected.
Albertsons store-made Tempura Shrimp with Thai Sweet Chili Sauce is being recalled because the contains statement does not declare shrimp. 14 units are affected.
Albertsons store-made Salmon Fillet Carne Asada Marinade is being recalled because the contains statement does not declare salmon. Six units are affected.
Philips Medical Systems is recalling 27 Philips Azurion 3M15 units because a software issue can cause unusable dark images during imaging procedures.
B. Braun CESK Riverside Health System kits are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering the product unusable.
Albertsons store-made Ready Meals Sandwich Haggie Store Classic Tuna is being recalled because the contains statement does not declare tuna.
Albertsons store-made Shrimp 41-50 P&D with Jamaican Jerk Marinade is being recalled because the contains statement does not declare shrimp. Two units are affected.
Albertsons store-made Gourmet Walnut Sticky Buns, 4 count, are being recalled because the contains statement does not declare walnut. 73 units are affected.
Xyvona levorphanol tartrate tablets, 2 mg, are being recalled following FDA's denial of marketing the product under the proprietary name Xyvona.
Albertsons store-made Ready Meals Brie Almond Tray Small is being recalled because the contains statement does not declare almond. Three units are affected.
Albertsons store-made Almond Raspberry Filled Croissants, 4 count, are being recalled because the contains statement does not declare almond. 15 units are affected.
Albertsons store-made Ready Meals Tuna Salad & Pepper Jack Cheese Snacker is being recalled because the contains statement does not declare tuna. 293 units are affected.
Albertsons store-made Shrimp Kabob 16-20 count with Kung Pao Marinade is being recalled because the contains statement does not declare shrimp.
DeRoyal Industries Inc. is recalling Covaderm Plus Vascular Access Dressings because they lack sterility assurance.
Covidien Mon-a-Therm general purpose temperature probes in size 9 Fr, REF 90050, are being recalled because the devices lack FDA clearance. 128,900 units are affected.
B. Braun Lyndon B Johnson Hospital spinal epidural kits are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering it unusable.