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 48,100 notices were distributed nationwide, so they reach Illinois too — those are in the archive.
Reported Feb 2, 2022
GAT SPORT JETFUEL DIURETIC; FOR RELIEF OF WATER WEIGHT GAIN; Muscle Defining Formula; Stimulant Free Natural Herbal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.World Health Products LLC
FDA (openFDA food enforcement)
Reported Jan 26, 2022
SonarMed AirWave Monitor Kit (Monitor, Sensor Cable, Power Cord), Item Code AW-M0001. used with endotracheal tube (ETT)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
FDA (openFDA device enforcement)
Reported Jan 26, 2022
greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring, non-ridged, 24 racks of 50…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greiner Bio-One North America, Inc.
FDA (openFDA device enforcement)
Reported Jan 26, 2022
KWIK-STIK 2 Pack, Catalog #0894P; KWIK-STIK 6 Pack, Catalog #0894K; and LYFO DISK, Catalog #0894L; Microsporum canis…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
FDA (openFDA device enforcement)
Reported Jan 26, 2022
VITROS Immunodiagnostic Products High Sample Diluent A Reagent Pack
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jan 26, 2022
1. Sensis, material # 10764561; UDI: 04056869010137 2. Sensis Vibe Hemo, material # 11007641; UDI: 04056869010199 3.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 26, 2022
Neodent Easypack Helix GM Acqua 3.5X8/Smart 4.5X2.5 -intended for dental implant Item 138.089
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straumann USA LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 19, 2022
Ki Mobility, Little Wave Tyke (Weight Limit: 95 lbs), Specifically the IFU The Little Wave Tyke is a manually operated…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ki Mobility LLC
FDA (openFDA device enforcement)
Reported Jan 19, 2022
Chili & Cheese Brat on Pretzel Bun, Item Number 1098, Net Wt. 6.5 oz(185g), UPC 7 47804-01098 8. Keep Refrigerated.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kitchen Fresh Foods, LLC
FDA (openFDA food enforcement)
Reported Jan 19, 2022
Medtronic Custom Perfusion kits, with the following product descriptions and corresponding model numbers: 1. CUSTOM…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
FDA (openFDA device enforcement)
Reported Jan 19, 2022
Boba Origin Brown-Sugar Milk Tea 100% WHEY PROTEIN ISOLATE 5.5g BCAA INGREDIENTS: Whey Protein Isolate, Black Tea,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.NutraCap Labs LLC
105 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 12, 2022
Simplexa Direct Amplification Disc Kit, Product Kit Code MOL1455
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiaSorin Molecular LLC
FDA (openFDA device enforcement)
Reported Jan 12, 2022
Flex-Thread Inserter Shaft intended for Fibula intramedullary-intended to be used with the Inserter Draw Rod and Blue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flower Orthopedics Corporation
FDA (openFDA device enforcement)
Reported Jan 12, 2022
DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medshape, Inc.
FDA (openFDA device enforcement)
Reported Jan 12, 2022
Atellica CH 930 Analyzer with Software version: V1.25.1 and lower- An automated, clinical chemistry analyzer designed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jan 12, 2022
iontoPATCH On-the-Go Patch Therapy, Transdermal Iontophoretic Drug Delivery System, Extra Strength, 8-HOUR Average Wear…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Tapemark Company
FDA (openFDA device enforcement)
Reported Jan 5, 2022
iDesign, Model - G300: System AWS (International), System AWS (China), Advanced WaveScan Studio (United States);…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AMO Manufacturing USA, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 5, 2022
RAPID 20 E, REF 20701, System for the identification of Enterobacteriaceae in 4 hours, 25 strips/package, IVD.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
FDA (openFDA device enforcement)
Reported Jan 5, 2022
da Vinci SP Surgical systems with the following Model Name/ Model Number / UDI: ASSY,PSS,SP1098,P4/ 380601-44/…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jan 5, 2022
Karl Storz Udel Sterilization Tray Instructions for Use, Tray Part Number/Description: 39301ACTS/CAMERA TRAY (STERRAD,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Dec 29, 2021
TruDi NAV Suction Instruments: 0-Degree, REF: TDNS000Z; 70-Degree, REF: TDNS070Z; and 90-Degree, REF: TDNS090Z
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acclarent, Inc.
FDA (openFDA device enforcement)
Reported Dec 29, 2021
SYNCHRON Systems Cholesterol (CHOL) Reagent, REF: 467825
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Dec 29, 2021
WIRION EMBOLIC PROTECTION SYSTEM, Delivery Catheter and Filter and Retrieval Catheter, 6Fr, REF (Model Number) WRN-D6
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cardiovascular Systems Inc.
FDA (openFDA device enforcement)
Reported Dec 29, 2021
Leica Microsystems M220 F12 Microscope Systems
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, 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.