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 48,132 notices were distributed nationwide, so they reach Illinois too — those are in the archive.
Reported Jul 22, 2015
Diet Bubba Cola, 20 FL. OZ (1.25 PT) 591 mL INGREDIENTS: CARBONATED WATER, HIGH FRUCTOSE CORN SYRUP, CARAMEL COLOR,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dr. Pepper Snapple Group Inc.
FDA (openFDA food enforcement)
Reported Jul 22, 2015
RadiForce GX540, 5MP Monochrome LCD Monitor, Part Code No. 0FTD1826A5, 0FTD1826B5, 0FTD1826C5, UPC 690592034752. This…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eizo Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2015
MOSAIQ Oncology Information System MOSAIQ is an oncology information system used to manage workflows for treatment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Altiva / Exactech Spine, Large Set Screw, Catalog Number 28202, Lot Number AS05107. Intended to provide immobilization…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2015
CapriSun Variety Pack, with a multi colored plastic wrap with white and yellow lettering, covering 4 cartons. The 4…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kraft Foods North America
FDA (openFDA food enforcement)
Reported Jul 22, 2015
Allofix Insertion Kit, 2.0 mm, Single Drill, Product Usage: MTF Surgical Instruments are designed for the specific…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Musculoskeletal Transplant Foundation, Inc.
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Dual Delivery 4DD-1 of GYC-1000 Green Laser Photocoagulator system GYC4DD-1: The Nidek Green Laser Photocoagulator…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nidek Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Autopen Classic Automatic insulin delivery pen, 3.0ml x 2 unit 2-42 units, AN3800, Lot 7JH, NDC 08470-3800-01, The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Owen Mumford USA, Inc.
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Sorin Stockert Heater-Cooler 3T, 230 V Temperature control for extracorporeal perfusion of durations up to 6 hours.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group USA, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2015
0210-312-000-Woundcare Replacement kit with soft tip; 0210-318-000; Woundcare Replacement with fan tip; 0210-318-100-…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Jul 15, 2015
Foil bags containing 2.2 lbs. each of almond flavored powder and sold under the Boba Direct, Inc. brand.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boba Direct, Inc.
23 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 15, 2015
Garden Fresh Steakhouse Potato Salad Kit, CODE#1076, NET WT 10.75 LBS (4.876 KG) , UPC 0 01 11596 51076 4.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Garden-Fresh Foods, Inc.
FDA (openFDA food enforcement)
Reported Jul 15, 2015
Philips GoSafe Communicator 7000L Personal emergency response system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lifeline Systems, Incorporated
FDA (openFDA device enforcement)
Reported Jul 15, 2015
New Punjab Burfi is an Indian snack cut into 1lb or 0.5 lb. squares. Product is packaged in clear plastic container…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.New Punjab Sweets Inc.
6 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 15, 2015
Breast Pack - contains Devon Light Glove Used during surgery
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stradis Healthcare, LLC.
50 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro diagnostic.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Jul 8, 2015
HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac transplantation in patient who are at risk of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartWare Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Milestone Wand STA Handpiece for the delivery of local anesthesia to dental tissue. Model Number STA-5050-305. The Wand…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Milestone Scientific, Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2015
StoneLight 30 Laser System (NS3000). For use in surgical procedures using open, laparoscopic and endoscopic incision,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.New Star Lasers, Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Dr. Sheffield's LUBRI GEL 3 oz (85 g) Non sterile over-the-counter personal lubricant.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sheffield Pharmaceuticals, LLC
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Infinite F500, in vitro diagnostic. Product Usage: The Tecan Infinite F500 is a multifunctional microplate reader with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tecan US, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Natural Knee II Revision Femoral Stem, 125mm, item 6215-12-185. packaged in configuration 803/791. Knee Prosthesis…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2015
BLUE BELL COUNTRY COOKIE VANILLA ICE CREAM & CHOCOLATE CHIP COOKIE SANDWICH 5.75 FL OZ (170 mL)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Blue Bell Creameries, LP
285 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 1, 2015
LapSac Surgical Tissue Pouch. The current intended use for the LapSac Surgical Tissue Pouch is for isolating tissue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
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.