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 Aug 21, 2019
BD Vacutainer Fluoride Tubes for Blood Alcohol determinations Part Number: 367001 Product Usage: Blood Alcohol…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Aug 21, 2019
Entenmann's Little Bites Soft Baked Cookies (5 pack Mini Chocolate Chip variety) Net Weight of 5ct box 6.88oz. 5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BIMBO Bakeries USA Inc.
FDA (openFDA food enforcement)
Reported Aug 21, 2019
iGUIDE System with software build iGuide 2.2.0, 2.2.1, and 2.2.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Aug 21, 2019
Aries Bordetella Assay, REF 50-10037, UDI # 00840487101452
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 21, 2019
Medline Primary Warmer Pack, Product No. DYNJ52510A. The Medline Primary Warmer Pack contains the recalled Vyaire…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medline Industries Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 21, 2019
SLIM Handle - catalogue #: SLM-HND100 a component of Simple Locking Intramedullary (SLIM) System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pega Medical Inc.
FDA (openFDA device enforcement)
Reported Aug 21, 2019
The Cookie Dough Cafe - Chocolate chip chilled gourmet edible cookie dough; 1.6 oz bars, packaged in plastic wrappers,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Cookie Dough Cafe
FDA (openFDA food enforcement)
Reported Aug 21, 2019
Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151810
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2019
The Alinity ci-series System Control Modules which are configured with Alinity c Processing Modules. The Alinity…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
FDA (openFDA device enforcement)
Reported Aug 14, 2019
STERILE GRAVES VAGINAL SPECULUM MEDIUM Kit Code # GVS10MST - Product Usage:The speculum is used to spread the walls of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
12 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Great Value Mild Taco Seasoning, Net Wt. 1 OZ, Distributed by Wal-Mart Stores, Inc. Bentonville, AR. UPC 0 78742 24572v0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CH Guenther & Sons, Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 14, 2019
IDEAL IMPLANT Structured Breast Implant, saline breast implant, in the following sizes: 210cc, 240cc, 270cc, 300cc,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ideal Implant Incorporated
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Workstation, G2, Configured (P/N 000-0241)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intellijoint Surgical, Inc.
FDA (openFDA device enforcement)
Reported Aug 14, 2019
MED EL Cochlear Implant System, Mi1000 MED EL CONCERTO, sold under the following implant types: a. Mil000 CONCERTO PIN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MED-EL Elektromedizinische Gereate, GmbH
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Endoscopic Cleaning Brushes sold in various Endoscopy Kits - Product Usage: The brushes are used to help clean out the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Aug 14, 2019
SmartRelease Endoscopic Carpal Tunnel Release Handpiece (ECTR handpiece), part numbers 81014 and 83014
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MicroAire Surgical Instruments, LLC
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Ginger Spice, 1 oz (28.4 g), 2 oz, 4 oz, and 1-3 lb packages. An herbal tea, Taos, NM
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Milkweed & Monarch, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 14, 2019
The Visibly Online Refractive Vision Test which is part of the Visibly Vision Test Solution, This is a software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Opternative Inc.
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Human Assayed Multi-Sera Level 2, Model NO. HN1530 Product Usage: This product is intended for in vitro diagnostic use,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories, Limited
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Dimension¿ Ferritin (FERR) Flex¿ reagent cartridge DM FERR Product Usage: The FERR Flex reagent cartridge is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Lantis 6.1 Commander, Model # 5493072 - Product Usage: Lantis Treatstation is to allow the radiation therapist to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2019
ELLIPSE VR, REF: CD1377-36C Implantable cardioverter defibrillators (ICDs)
High riskUsing this product could cause serious injury, illness or death — stop using it now.St Jude Medical Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Shirakiku FISH CAKE IWASHI TEN SK F 20/150 g; Net WT. 5.29 oz. Keep frozen, 7 pcs. UPC 074410925246 Distributed by…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wismettac Asian Foods, Inc.
7 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 7, 2019
GE Senographe Pristina - Product Usage: Senographe Pristina generates digital mammographic images that can be used for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
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.