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 Nov 11, 2020
Model 3300 LATITUDE Programming System with installed Model 3892 ALTRUA, INSIGNIA I, NEXUS I Software Support…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Nov 11, 2020
Aestiva/5 MRI Anesthesia System - Product Usage: The Aestiva/5 MRI Anesthesia System provides the functional feature…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 11, 2020
metformin HCL ER 500 mg, a) 30 tablets NDC: 72789-009-30; b) 60 tablets NDC: 72789-009-60; c) 90 tablets NDC:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PD-Rx Pharmaceuticals, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Nov 11, 2020
Ultra2 Resolution Variants System for Abnormal Hemoglobin Quantitation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Primus Corporation
FDA (openFDA device enforcement)
Reported Nov 4, 2020
CMEAmerica BodyGuard Wall Charger: Lot number 2019-0364, Mode/Catalogue number 151-143XL, *+B 01151143X…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CME America LLC
FDA (openFDA device enforcement)
Reported Nov 4, 2020
Revolution Apex, Revolution CT with Apex Edition, Model 5995000-5 - Product Usage: The system is intended for head,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Nov 4, 2020
Eishindo brand "CUP JELLY (MINI); NET WT. 28.2oz (800g); 50pcs; INGREDIENTS: WATER, HIGH FRUCTOSE SYRUP, APPLE JUIC,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hadson (Toko) Trading Co., Inc.
FDA (openFDA food enforcement)
Reported Nov 4, 2020
Merge LIS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Nov 4, 2020
Happy Tot Superfoods Gluten Free Oat Bar Organic Blueberries & Oatmeal. SKU: TB-BLOT-5 and TB-BLOT-5-WM. Ready-to-eat…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nurture Inc. dba Happy Family
2 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 4, 2020
5.5MM Arthrogarde Hip Access Cannula
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Oct 28, 2020
BD Nexiva Closed IV Catheter System Dual Port (20 GA 1.75 IN) Catalog (Ref) No. 383538 BD Nexiva closed IV catheter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Oct 28, 2020
NanoClave Connector; 1 unit per pouch, 100 multivac pouches per case;UDI (01)10887709051017(17)241201(30)100(10)4549051;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
98 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2020
MR Coils The MR Coil is intended to be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Invivo Corporation
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Olympus CHF-CB30S Choledoscope Intended Use: The device was designed to be used with an Olympus TV camera system, light…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen FIA is a lateral flow immunofluorescent sandwich assay…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quidel Corporation
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Genesis (GII) - Product Usage: designed for use in patients in primary and revision surgery, where the posterior…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
40 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Trevo XP ProVue Retriever, REF (Size): 90182 (4MM x 20MM); 90185 (4MM x 30MM); 90186 (6MM x 25MM). Procedure Pack REF:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Stryker Neurovascular
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Marketside brand Cranberry Walnut Salad in 4.5 oz. plastic bowl with poly film lidding (6 bowls per case). UPC:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Taylor Farms Tennessee, Inc.
FDA (openFDA food enforcement)
Reported Oct 28, 2020
Langston Dual Lumen Catheter
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Shirakiku brand Black Fungus (Kikurage); 5 lb. bag, 6 x 5 lb. bags per case Item # 60403; UPC 0 74410 60403 5…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wismettac Asian Foods, Inc.
FDA (openFDA food enforcement)
Reported Oct 21, 2020
Alcon Custom-Pak Surgical Procedure Packs containing Cardinal Health" PROTEXIS" Latex Micro Surgical Gloves - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research, LLC
FDA (openFDA device enforcement)
Reported Oct 21, 2020
Smart Care HAND SANITIZER, Ethyl Alcohol 62%, packaged in 0.84 FL.OZ (25 mL), labeled as a) Paw Patrol (Item #:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ashtel Studios, Inc.
FDA (openFDA drug enforcement)
Reported Oct 21, 2020
Watermelon 10 oz UPC Code: 681131180672; Watermelon 32 oz UPC Code: 681131180689; Watermelon Chunks 42 oz UPC Code:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Country Fresh Inc.
15 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 21, 2020
Aquas PowerFlow Tube Set - Product Usage: The device delivers sterile irrigation fluids to surgical sites during…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Genicon, Inc.
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Illinois recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Other states
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.