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 Feb 4, 2015
Airo Mobile Intraoperative CT I Airo; Model #: MobiCT-32. Computed Tomography x-ray system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mobius Imaging, LLC
FDA (openFDA device enforcement)
Reported Feb 4, 2015
Verasense Knee System, Model SYK-TRCR 02. Intelligent disposable tibial insert that measures dynamic loads during…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthosensor, Inc.
FDA (openFDA device enforcement)
Reported Feb 4, 2015
Thera Tablets with Beta Carotene Dietary Supplement
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The Harvard Drug Group, LLC
FDA (openFDA food enforcement)
Reported Feb 4, 2015
Market Pantry Brand Dark Chocolate Covered Almonds 9 oz., UPC 085239555644
High riskUsing this product could cause serious injury, illness or death — stop using it now.Zachary Confections, Inc.
FDA (openFDA food enforcement)
Reported Jan 28, 2015
FLUTTER Percussor respiratory device, packaged one unit per clear plastic package. Product Usage: Product is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aptalis Pharmatech Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2015
Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Jan 28, 2015
PF4 Concentrated Wash (10x), REF 403624, packaged in the following assay kits: 1. ImmucorGamma LIFECODES PF4 IgG…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Genetic Testing Institute,Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2015
Philips IntelliVue TcG10; Monitor, carbon-dioxide, cutaneous. The IntelliVue TcG10 is a device for the measurement of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2015
Ysio Max, Luminos dRF Max and Agile Max systems with software version VE10 and SmartOrtho license. The Ysio Max is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 23, 2015
Illinois Firm Recalls Chicken Steak Products Due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Illinois Firm
USDA FSIS
Reported Jan 21, 2015
The Abbott m2000sp is an automated system for performing sample preparation for nucleic acid testing.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Molecular
FDA (openFDA device enforcement)
Reported Jan 21, 2015
MUM-1 (Multiple myeloma oncogene-1), catalog number PRM352 AA; Product Usage: For In Vitro Diagnostic Use. This…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biocare Medical LLC
FDA (openFDA device enforcement)
Reported Jan 21, 2015
iPlan RT Dose is a stereotactic radiation treatment planning system that is intended for use in stereotactic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Florida Firm Recalls Beef, Chicken and Pork Products Due to Misbranding and Undeclared Allergen
High riskUsing this product could cause serious injury, illness or death — stop using it now.Florida Firm
USDA FSIS
Reported Jan 21, 2015
MENTOR MemoryGel Resterilizable Gel Sizer Moderate Plus Profile STERILE. Breast prosthesis sizer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mentor Texas, LP.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Phadia 1000 Instrument (introduced as UniCAP 1000), Article number: 12-3800-01 (All instrument software versions since…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phadia US Inc.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Various Brilliance and Ingenuity Computed Tomography X-ray systems; one unit per package Product Usage: Intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Hors D'Oeuvre, Holiday Foods¿ Breaded Macaroni & Cheese Bites (item number 4802280). UPC 70220748022808, Keep Frozen,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Schwan Food Company dba Holiday Foods
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 21, 2015
EXp Tibial Insert ; Intended Use of Device(s): The Proven Gen-Flex Total Knee System is intended for: a. Total knee…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stelkast Co.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Drill set long, drill stop compatible for 4.8mm diameter implant, Article Number 040.447S Endosseous dental implant…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straumann USA, LLC
FDA (openFDA device enforcement)
Reported Jan 21, 2015
The SurgiCounter Charging Cradle Product Usage: SurgiCounter Charging Cradles are designed to be used with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform ophthalmic surgeries.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ziemer USA Inc.
FDA (openFDA device enforcement)
Reported Jan 14, 2015
Abdallah Milk Chocolate Bites CARAMEL, Net Wt 4.5 oz. (127g), UPC 7 6668407116 2, Ingredients: Pure milk chocolate…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abdallah Candies, Inc.
FDA (openFDA food enforcement)
Reported Jan 14, 2015
CSA Medical truFreeze System; Model: CC3-01, a cryogenic surgical device ***The involved units are those with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CSA Medical
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.