Recalls distributed in Illinois
These notices name Illinois in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
5,761 stored notices name Illinois, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Illinois too — those are in the archive.
Reported Feb 5, 2020
Custom Healthcare Systems, Inc. Inpatient Dialysis Kit PAK-19244. Single use. Dialysis kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Custom Healthcare Systems, Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2020
Sienna Chocolate Turtle Brownie (frozen); 108 OZ (6.75 LB) Uncut, 4 trays per case; UPC: 93901541857 SSC:10093901541854
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dianne's Fine Desserts
FDA (openFDA food enforcement)
Reported Feb 5, 2020
CS5/5+ Fastpacks, 225 mL, 150¿ Res Autotransfusion Device - Product Usage: its related accessory components are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Haemonetics Corporation
21 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 5, 2020
Ingredion ULTRA-TEX4 Food Starch in 50lb paper bags, product code 32166102CA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ingredion Incorporated
FDA (openFDA food enforcement)
Reported Feb 5, 2020
Jeni's Dairy Free Cold Brew with Coconut Cream Pints frozen dessert
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jeni's Splendid Ice Creams LLC
FDA (openFDA food enforcement)
Reported Feb 5, 2020
Healon GV PRO 0.85 mL, Model (U.S.): 10-2400-14, Model (O.U.S.): 10-2705-14, 10-2715-14, 10-2725-14, and 10-2755-14
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2020
AQURE basic sytem, FLEXLINK, REF 933-599, Version: 2.3.3 (17), CE IVD, Rx Only, UDI: (01)05700699335999 Intended use:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Feb 5, 2020
RayStation stand-alone software treatment planning system. Models 4.0, 4.3, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Feb 5, 2020
Cobas infinity central lab / cobas infinity core license-a Calculator/Data Processing Module, For Clinical Use Material…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Jan 29, 2020
TruDi NAV Suction, TDNS000Z, 0 Degree Tip Angle, (01)10705031245877
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acclarent, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2020
VACUETTE TUBE, 3.5mL CAL Serum Sep Clot Activator, REF 454067P - Product Usage: VACUETTE Tubes, Holders, and Needles…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greiner Bio-One North America, Inc.
FDA (openFDA device enforcement)
Reported Jan 29, 2020
Imactis Navigation Kit, REF 10100, Content Sterile Needle Holder Ref. A10010 CE 0459, Sensor Cover Ref. PC3688 CE 0482,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Imactis
FDA (openFDA device enforcement)
Reported Jan 24, 2020
Amity Packing Company Inc. Retira Productos De Carne Molida Cruda Debido A Una Posible Contaminación Con Materia Extraña
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amity Packing Co. Inc.
USDA FSIS
Reported Jan 22, 2020
HOME CHEF HEAT & EAT Baked Macaroni & Cheese NET WT. 12 oz (340G) keep refrigerated, Distributed by: The Kroger Co.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bakkavor Foods USA Inc.
FDA (openFDA food enforcement)
Reported Jan 22, 2020
RTE bacon and eggs 3.6 oz package
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cheesewich Factory
FDA (openFDA food enforcement)
Reported Jan 22, 2020
ADVANCED ENDOSEE System CANNULA, Cooper Surgical Product Code/Model Number: ESPX5 The Advanced Endosee Cannula…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2020
Medline Thermistor Foley Catheter 14 FR 5-10 ml, non sterile Catalog Number: 102201101463MD {Medline code 55346)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Degania Silicone, Ltd.
FDA (openFDA device enforcement)
Reported Jan 22, 2020
QuickDraw Venous Cannula, REF: QD22, UDI: 00690103182699; and REF: QD25, UDI: 00690103182705
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Jan 22, 2020
Butler's Dark Chocolate with Irish Whisky, 3.52oz bar, UPC 8 44984 17619 7, 10 units per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gourmet International Ltd.
FDA (openFDA food enforcement)
Reported Jan 22, 2020
LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2020
Riverpoint Medical 18G Brachy Grid, B&K style, REF RPG-18, Sterile, Rx. The firm name on the label is Riverpoint…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Riverpoint Medical, LLC
FDA (openFDA device enforcement)
Reported Jan 22, 2020
Siemens ARTIS pheno, Model # 10849000. Interventional Fluoroscopic X-Ray System - Product Usage: Angiography system for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2020
Eczema Skin Relief Lotion, 2% Colloidal Oatmeal Skin Protectant Lotion, NET WT 14 OZ (396 g), NDC 65365-266-01,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sigan Industries Inc.
FDA (openFDA drug enforcement)
Reported Jan 22, 2020
Teleflex MEDICAL RuSCH One piece Male External Regular Catheter W/O Tape, REF A1500
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teleflex Medical
1 more product in this recall
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.