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 Dec 9, 2020
REF MC330209 6' (15 cm) Appx 0.09 ml, Smallbore Trifuse Ext Set w/3 MicroClave Clear, 0.2 Micron Filter, 1.2 Micron…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
FDA (openFDA device enforcement)
Reported Dec 9, 2020
YAGUMO AMANATTO GIFT BOX 6P 6/19.01 OZ JAN Code: 49 03089 39050 4 Imported by JFC International Inc. Los Angeles, CA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.J F C International Inc.
FDA (openFDA food enforcement)
Reported Dec 9, 2020
B. Braun Introcan Safety IV Catheters, Product codes REF 4252500-01 4252519-01 4252535-01 4252560-01 4252586-01…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Janus Trade Group
FDA (openFDA device enforcement)
Reported Dec 9, 2020
Tanimura & Antle brand Romaine lettuce. 1 head 12,15,018 and 24 case Product of USA UPC: 2-27918 20314-9 Tanimura &…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tanimura & Antle
FDA (openFDA food enforcement)
Reported Dec 9, 2020
BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Dec 2, 2020
AB PowerCel 230 (velvet black), REF: CI-5523-150, UDI: (01) 07630016832956 used to power the following devices: Na¿da…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Advanced Bionics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 2, 2020
Titan Pump - Product Usage: indicated for male patients suffering from erectile dysfunction (impotence) who are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coloplast Manufacturing US, LLC
FDA (openFDA device enforcement)
Reported Dec 2, 2020
EMPOWR Partial Knee Peg Drill Guide; Model: 800-06-007.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 2, 2020
Life2000 Ventilation System, including Life2000 Ventilator and Life2000 Compressor, Model MS-01-0118 - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom Manufacturing, Inc.
FDA (openFDA device enforcement)
Reported Dec 2, 2020
Box Label: ION Fully Articulating Catheter, REF 490105, VER 08 - Product Usage: used to navigate the Ion Fully…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Dec 2, 2020
ViewRay MRIdian System: Model No. 10000, CE, Rated Supply Voltage - 380/480 VAC, 3 - Frequency Range (Hertz) - 50/60…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Viewray, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 25, 2020
Art Of Tea - Feel Better tea; Produced and Distributed by: Art of Tea LLC, Monterey Park, CA Directions: 1 Tbsp of tea…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Art Of Tea
FDA (openFDA food enforcement)
Reported Nov 25, 2020
Catalog 314-13-23, Equinoxe Cage Glenoid, Posterior Augment, Left, Medium
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 25, 2020
VNS Therapy¿ AspireSR¿ Generator
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Nov 25, 2020
COAPTITE Injectable Implant, injectable, sterile, non-pyrogenic implant composed of spherical particles (75-125 microns…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merz North America, Inc.
FDA (openFDA device enforcement)
Reported Nov 25, 2020
Elastic Traction Device, 11mm Lower. UPN: ER56041 Reference Number: ETD-D-26-235-C-N - Product Usage: indicated for use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Micro-Tech USA
FDA (openFDA device enforcement)
Reported Nov 25, 2020
Trader Joe's brand Gluten Free Battered Halibut, SKU 00503822. Product of USA. Frozen product is packed in plastic bag…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Orca Bay Foods LLC
FDA (openFDA food enforcement)
Reported Nov 25, 2020
Artis zee floor, Artis Q ceiling, Artis Q.zen ceiling. Image-Intensified Fluoroscopic X-Ray System. Material numbers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Nov 25, 2020
Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thomas Scientific
FDA (openFDA device enforcement)
Reported Nov 18, 2020
SUNG HWAN E&B VIVACE Shenb Innovation of Beauty Technologyt - Product Usage: intended for use in the dermatologic and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesthetics Biomedical, Inc.
FDA (openFDA device enforcement)
Reported Nov 18, 2020
EDI Novel Coronavirus COVID-19 IgG ELISA Kit, REF: KT-1032 Per label: This kit is intended for qualitative detection of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Epitope Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 18, 2020
FRESH FROM MEIJER CANTALOUPE CHUNKS LARGE BOWL, 32oz Clear plastic container, UPC 219323109721. FRESH FROM MEIJER…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Meijer Inc./Traffic Dept.
11 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 18, 2020
OsteoBridge Intremedullary Knee Arthrodesis (IKA) nails
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merete Medical GmbH
3 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 18, 2020
Niobe ES System, Models 001-006000-1 and 001-006100-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stereotaxis 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.