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 48,123 notices were distributed nationwide, so they reach Kentucky too — those are in the archive.
Reported Jun 22, 2016
Piccolo Composite Tibia and Femoral Nailing Systems - Ball Tip Guide Wire for fixation of fractures that occur in and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CarboFix Orthopedics, Ltd.
FDA (openFDA device enforcement)
Reported Jun 22, 2016
TranSmart, Ginger Cookie, 300-1.2oz Cookies, Net Weight 22.5 lbs/10.22 kg (Frozen).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CSM Bakery Products NA
41 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 22, 2016
The XN-Series modules (XN-10, XN-20) are quantitative multi-parameter automated hematology analyzers intended for in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sysmex Corporation
FDA (openFDA device enforcement)
Reported Jun 22, 2016
Dome Centric component (Reference 01.04227.005) from the Anatomical Shoulder (AS) System 2.0. The Dome Centric connects…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer GmbH
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Wylwood Fresh Frozen Broccoli Cuts, NET WT. 16 OZ Code: A25335P and A15335P Dist By: Save-A-Lot Stores, Earth City, MO.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Alimentos Congelados, S.A. (Pinula)
FDA (openFDA food enforcement)
Reported Jun 15, 2016
4 ml FX Sodium Fluoride/Potassium Oxalate tube, Ref 454297 VACUETTE Glycolytic Inhibitor Tubes contain an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greiner Bio-One North America, Inc.
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Philips Healthcare DigitalDiagnost stationary X-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Healthcare
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Maestro Air Motor Pneumatic cranial drill motor. The Maestro Air Pneumatic System is a pneumatically operated surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Sterile Sheridan/HVT Cuffed, Murphy Eye, Tracheal Tube, Ref: V5-10314, ID: 7.0 mm, Rx Only, Manufactured by: Teleflex…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Persona Trabecular Metal Tibia; Persona Trabecular Metal Tibial Plate Instruments and Modular Brackets; Used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite Valve Product Usage: Used for aspiration of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Monaco RTP System Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2016
HAWAIIAN DELIGHT ING: IMITATION SOUR DRESSING, PEACHES, PINEAPPLE, MANDERIN ORANGES, SUGAR CHERRIES KEEP REFRIGERATED…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Frank L Harter & Sons Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 8, 2016
Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Angel Wings Complete Daily Multi with 146 nutrients including Anti-aging and Superfruit Antioxidants and 75 Plant…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Liquid Assets Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 8, 2016
Brilliance 64 Computed Tomography X-ray Systems Product Usage: Intended to produce cross-sectional images of the body…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Dimension Vista 500 Intelligent Lab System running on software versions V.3.6.1 SP1 or V.3.6.2, Device listing #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Reprocessed Microline Scissor Tips intended to be used with a reusable hand piece and designed for minimally invasive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sterilmed, Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Kroger CRANBERRY DELIGHT TRAIL MIX NET WT 14 OZ INGREDIENTS: DRIED CRANBERRIES ***ALMONDS, SUNFLOWER SEEDS*** UPC 0…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 1, 2016
WHIN Infusion Set - 90 Huber Needle and Wing (22 ga/1in). Intravenous delivery through intravascular ports, 20 units…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported Jun 1, 2016
ABG-HM-1 Hummi Micro Draw Blood Transfer Device Product Usage: It is used for blood transfer and collection from…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hummingbird Med
FDA (openFDA device enforcement)
Reported Jun 1, 2016
3.2 mm Three-fluted drill bit, sterile, Catalog ID # 03.010.060S Product Usage: Usage: The 3.2 mm Three-fluted Drill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 25, 2016
Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diamedix Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 25, 2016
Lumenis M22 System Model Number: GA-0005400 (M22 IPL + YAG Module) with Acne Filter (KT-1014971).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lumenis Ltd.
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.