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 Aug 26, 2026Updated Sep 13, 2026
Organic Whole Blueberries, Net Wt 10 oz (284g) plastic bag, packed in 8 bags per case of 10 oz each. Keep Frozen UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Publix Super Markets, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 26, 2026Updated Sep 7, 2026
Dentsply Sirona Capsule Mixer Model No. 5546068
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SDI Limited
FDA (openFDA device enforcement)
Reported Aug 26, 2026Updated Sep 7, 2026
Whole Foods Medium Pico de Gallo Guacamole Dip, Keep Refrigerated. Packed in various sized clear plastic containers.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.WFM Purchasing, LP
9 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 19, 2026Updated Sep 7, 2026
ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Erbe USA Inc.
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US MV-BGA01095 For use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microvention Inc.
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OBP Medical Corporation
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Sep 14, 2026
Cibus Fresh, Sprig & Sprout, and Jack & Olive brand Garden Salad, 7.75oz clear plastic container, UPC 810028250253
High riskUsing this product could cause serious injury, illness or death — stop using it now.Piazza Produce (dba CIBUS Fresh)
FDA (openFDA food enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 Software Version: N/A Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
GM Helix Implant, Endosseous Dental Implant Article No. 109.984
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 Aug 19, 2026Updated Sep 7, 2026
MARKETSIDE ICEBERG SALAD 10/24 oz, UPC 681131328951; MARKETSIDE ICEBERG SALAD 12/12 oz, UPC 681131328944; MARKETSIDE…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Taylor Farms de Mexico S. de R.L. de C.V.
20 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
navify Digital Pathology (on-prem) v2.5, Material Number 10092343001 navify Digital Pathology (Cloud) v2.5. Material…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Aug 12, 2026
REF # D23352, MicroScan LabPro V5.03 Panel Update 11 (US), Electronic installed on the following instruments: -…
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 Aug 12, 2026
FilmArray NGDS Warrior Panel REF NGDS-ASY-0007 UDI-DI code: (01)00851458005136 The FilmArray NGDS Warrior Panel is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biofire Defense
FDA (openFDA device enforcement)
Reported Aug 12, 2026
Radial Jaw 4 Standard Capacity Biopsy Forceps with the following descriptions and UPN: 1. Radial Jaw 4 SC 240cm Box 20;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 12, 2026
Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection (Neuroguard IEP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Contego Medical, Inc.
FDA (openFDA device enforcement)
Reported Aug 12, 2026
Blom-Singer Classic Indwelling Voice Prosthesis, 16Fr/10 mm REF: 1610-LEF
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Freudenberg Medical, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 12, 2026
GEM Premier 7000 with iQM3 Part Numbers: 00077407508 00077407510 00077415004 00077415008 00077415010 00077430010…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Laboratory
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 12, 2026
Spicy Breakfast Burrito sold under the following brand names: FRESH & READY FOODS Spicy Breakfast Burrito Net Wt. 8.2…
High riskUsing this product could cause serious injury, illness or death — stop using it now.M.G. Foods, Inc.
FDA (openFDA food enforcement)
Reported Aug 12, 2026
Brand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number: Quantum 4Front 2 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pride Mobility Products Corp.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026Updated Sep 16, 2026
Sainforage Sainfoin + Grass + Alfalfa Forage Pellet 40 lb (18.14 KG) UPC: 720260672693. Packaged BOPP woven plastic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fundamental Feed
2 more products in this recall
FDA (weekly enforcement report)
Reported Aug 5, 2026Updated Sep 16, 2026
Immune Globulin (Human); Octagam IVIG 10% 30gm/300mL (Batch KP12B8561)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Octapharma Pharmazeutika Produktionsgesellschaft m.b.H.
FDA (weekly enforcement report)
Reported Aug 5, 2026
Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Permobil Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026
Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory…
High riskUsing this product could cause serious injury, illness or death — stop using it now.ResMed Ltd.
FDA (openFDA device enforcement)
Reported Jul 29, 2026
Power F2 Powered Fastening System, Product No. 0567091 Powered fastening system intended for professional use only.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ferno-Washington 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.