Recalls distributed in Kentucky
These notices name Kentucky 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.
3,340 stored notices name Kentucky, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Kentucky too — those are in the archive.
Reported Apr 19, 2023
Frisch's Tuna Salad packaged in 4lb plastic tubs - sold individually
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fkc LLC
FDA (openFDA food enforcement)
Reported Apr 19, 2023
White Castle Chicken Slider Individual sandwiches packaged as two sandwiches - 16 packages per case Unit Size…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.White Castle System
FDA (openFDA food enforcement)
Reported Apr 12, 2023
Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath, 8.5F(Small), REF D-1385-01-S, RX CE 2797, Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosense Webster, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 12, 2023
Peanut Butter Pie, 1 count
High riskUsing this product could cause serious injury, illness or death — stop using it now.Desserts by Helen, Inc.
FDA (openFDA food enforcement)
Reported Apr 12, 2023
Astor Chocolate Wafer Stick NWT WT. 11.64 OZ 330g UPC 72375102886
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eastland Food Corporation
FDA (openFDA food enforcement)
Reported Apr 12, 2023
Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by clinicians and medically qualified…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remote Diagnostic Technologies Ltd.
FDA (openFDA device enforcement)
Reported Apr 5, 2023
Alcon Custom Pak Surgical Procedure Pack: Pak Number & Pak Description: 17533-04 DR GROSS LPS LLC 18704-03 CATARACT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research, LLC
FDA (openFDA device enforcement)
Reported Apr 5, 2023
Color Cuff Single Port, Single Bladder 30 (Royal Blue) Quick Connect, REF: 5921-030-135; Color Cuff Dual Port, Single…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Apr 5, 2023
ISH Shrimpish Sample Meal Kit: ( Sample Meal Kit ) a package containing two ISH Foods plant-based Shrimpish products…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Ish Company
FDA (openFDA food enforcement)
Reported Mar 29, 2023
BD Pyxis Anesthesia ES System (PAS ES), REF: 327; BP Pyxis MedStation ES (Med ES Main), REF: 323; BD Pyxis MedStation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Mar 29, 2023
DG Health brand Sugar Free Daily Fiber in 10 oz. plastic containers (UPC: 860005934294).
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dollar General Corporation
FDA (openFDA food enforcement)
Reported Mar 29, 2023
Russel Stover Sugar Free Peanut Butter Cups packaged in 2.4oz peg bag, containing individually wrapped pieces. UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Russell Stover Candies Inc.
FDA (openFDA food enforcement)
Reported Mar 22, 2023
Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM, REF: 1610MSK; 18G x 16CM, REF: 1816MSK
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Mar 22, 2023
Brainlab ExacTrac Dynamic software, Medical Charged-Particle Radiation Therapy System, model 20910-01E and 20910-01F.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Mar 22, 2023
Fruit flavored ready-to-eat cereal packaged in 1.27 oz. (UPC 850017468214) and 8oz. ( UPC 850017468085) plastic stand…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Catalina Snacks
6 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 22, 2023
DF FT Simple Free Dark Wafer (MB), Item # 12957. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Sugar, Palm…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Clasen Quality Chocolater, Inc.
17 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 22, 2023
YoCrunch Vanilla Lowfat Yogurt with M&Ms 6 oz (170g) UPC 046675000792 packaged in plastic cup with self-contained…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Danone US LLC
FDA (openFDA food enforcement)
Reported Mar 22, 2023
Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keurig Dr Pepper
FDA (openFDA food enforcement)
Reported Mar 22, 2023
ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mead Johnson & Company
FDA (openFDA food enforcement)
Reported Mar 15, 2023
Brussel Sprouts 98.5% of product was packaged for retail and 110 cases were bulk Brands: 4 Earth Farms, Trader Joe s,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.4 Earth Farms formerly Mcl Fresh Inc.
FDA (openFDA food enforcement)
Reported Mar 15, 2023
LATITUDE NXT Remote Patient Management System, LATITUDE NXT System Server Software Model 6460.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Mar 15, 2023
Simplexa COVID-19 Direct, REF: MOL4150; including Reaction Mix, REF: MOL4150; with previous assay definition v2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiaSorin Molecular LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 15, 2023
Given Imaging SmartBar Cereal Bar; Net Weight 2.53 oz (72 g); Ingredients: glucose syrup, soy crisps, oats, pea…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Given Imaging Ltd.
FDA (openFDA food enforcement)
Reported Mar 15, 2023
Sprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and 1ES211-1.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Linet Spol. S.r.o.
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.