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 Feb 18, 2026
Ore-Ida Tater Tots shaped potatoes, item number OIF00215A. Frozen potato product is packaged in clear unlabeled poly…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McCain Foods USA Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 18, 2026
Spicy Breakfast Burrito in a flour tortilla. Net Weight 10 oz (283g) Scrambled eggs, Salsa, Potatoes, Jalapenos,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MG Foods-Compass Group
FDA (openFDA food enforcement)
Reported Feb 18, 2026
Brilliance iCT; Product Code (REF): 728306;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 11, 2026
Repackaged M&Ms Peanut candies, Net Wt 1.3 oz. Item BB471BG. Labeled as Make Your Mark. For nutrition facts information…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beacon Promotions Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 11, 2026
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 11, 2026
Product Name: Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Model/Catalog Number: CL0073 Software Version: Not…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fujirebio Diagnostics, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 11, 2026
Brand Name: Da Vinci Product Name: da Vinci X, Xi Surgical System, & da Vinci 5 Surgical System Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Feb 11, 2026
MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software Version 6.60 The MiniMed 780G insulin pump…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Feb 11, 2026
Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens, Catalog VFD 2. Volk Magnifying Lens, Catalog VMD
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vortex Surgical Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 4, 2026
Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LimFlow, Inc.
FDA (openFDA device enforcement)
Reported Feb 4, 2026
Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count bottle, BIO7772 120 count…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quten Research Institiute LLC
FDA (openFDA food enforcement)
Reported Jan 28, 2026
The LDL-Cholesterol assay is comprised of two distinct phases. In phase one a unique detergent solubilizes cholesterol…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Ireland, Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2026
Brand Name: EDAN Product Name: Fetal Monitor Model/Catalog Number: F2, F3 Product Description: The devices are bedside…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edan Diagnostics
15 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 28, 2026
SQ40S Blood Transfusion Filter
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GVS TM, Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2026
Tego Connector: REF: 011-D1000, 01C-D1000, 055-D1000, D1000; Conector Tego: REF: LAT-D1000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 28, 2026
Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Bag Model/Catalog Number: 490127 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2026
Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Reference Numbers: ENDO-AN2030/B IN4130/CNK IN4130/H…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2026
2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8
Moderate riskThis product could cause temporary or reversible health problems — stop using it.House Of Flavors, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 21, 2026
da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073 (2.7-4cm,SP1098, Box) & 430075…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jan 21, 2026
Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Tomography (CT) X-ray System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mobius Imaging, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2026
CentriMag Blood Pump, REF: 102953, 201-20003, 201-90010, 201-90016; CentriMag RVAD HDE KIT, REF: 104318; CentriMag…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec LLC
FDA (openFDA device enforcement)
Reported Jan 14, 2026
BD Pyxis ES Enterprise Server Catalog Numbers 1115-00, 137672-02,137672-03 137671-02, 137671-03, 137670-02, 137670-03,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jan 14, 2026
EverRoast Chicken Caesar Salad 850042244142 Net Wt: 8.5 oz (255g)
High riskUsing this product could cause serious injury, illness or death — stop using it now.GBC Food Services, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 14, 2026
Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR Basic Kit is indicated when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp. (NeuroSciences)
1 more product in this recall
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.