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 48,122 notices were distributed nationwide, so they reach Kentucky too — those are in the archive.
Reported May 28, 2014
SW-2008 Snuggle Warm Sterile Cardiac Connective Warming Blanket; used with the Equator Convective Warmer, are intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
FDA (openFDA device enforcement)
Reported May 21, 2014
HeartWare HVAD Pump Implant Kit (Heartware Ventricular Assist Device) - HeartWare Battery For use as a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartWare Inc.
FDA (openFDA device enforcement)
Reported May 21, 2014
Private Selection Chocolate Hazelnut Mascarpone Ice Cream, 16 fl oz lamented carton. Product labeled in part, "PRIVATE…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kroger Co.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 21, 2014
Recalled product is a component of the Newport Medical Instruments e360 Ventilator: single board computer, part number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nellcor Puritan Bennett Inc. (dba Covidien LP)
FDA (openFDA device enforcement)
Reported May 14, 2014
Bissinger's Dark Chocolate Bunny Ears, 1 oz, individually wrapped in clear plastic with an ingredient card insert and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Karl Bissinger LLC
FDA (openFDA food enforcement)
Reported May 14, 2014
PRIVATE SELECTION SWEET STRAWBERRY SORBET, Labeled in part: "INGREDIENTS: WATER, SUGAR***DISTRIBUTED BY, THE KROGER…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kroger Co.
FDA (openFDA food enforcement)
Reported May 14, 2014
Mar Cor Purification, Central Water Platform (CWP), 102, 104 and 106. Product Usage: The CWP is a Central reverse…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mar Cor Purification
FDA (openFDA device enforcement)
Reported May 7, 2014
HexaPOD evo RT Couchtop. To support and aid in positioning a patient during radiation therapy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported May 7, 2014
Abbott Acclaim Infusion Pump Designed to deliver parenteral infusions including whole blood or red blood cell…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Amo-O Herbal Stimulator, 2 fl. oz. Manufactured by Meta Labs, Alpharetta, GA 30076, UPC Code 80702-1 Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Altasource LLC dba Meta Labs LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Jolly Time Microwave popcorn, Butter, 3/3-oz bags/carton. The cartons are packaged 12-cartons/case. Individual carton…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Pop Corn Co.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 30, 2014
ZYM B Reagent (REF 70493). The ZYM B reagent is an additional test used to reveal the results of some miniaturized…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device) Catalog Numbers: 1100, 1101, 1102, 1103, 1104,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare Inc.
FDA (openFDA device enforcement)
Reported Apr 30, 2014
LifeShield LATEX-FREE HemoSet 100 mL Burette I.V. PlumSet, Nonvented, 105 inch with Prepierced Reseals, OPTION-LOK and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2014
VITROS Chemistry Products CDM PROM (Calibration Data Module) No. 0168, Catalog Number/REF 199 9077, used in conjunction…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Apr 30, 2014
MULTIX FUSION. The Multix Fusion system is a radiographic system used in hospitals, clinics, and medical practices.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Stryker PenAdapt"; Rx Only, Sterile. This device is an accessory to an electrosurgical unit (ESU). The PenAdapt is used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Monofilament and Multifilament Non-absorbable Steel Suture; Product Codes: 0520197-2, 29-727, 29-7270M4, 29-7281M4,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 25, 2014
Kentucky Firm Recalls Pork Products Due To Misbranding And Undeclared Allergen
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Knockum Hill Bar-B-Que
USDA FSIS
Reported Apr 23, 2014
Brilliance CT 16, Brilliance CT 64, Brilliance CT Big Bore Oncology, Brilliance CT Big Bore Radiology, Brilliance iCT,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 23, 2014
Graeter's Ice Cream Big Scoop COOKIES AND CREAM Ingredients: cream, milk, cane sugar***locust bean gum. Manufactured…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tedesco LLC
FDA (openFDA food enforcement)
Reported Apr 16, 2014
Economy Elastic Knee Sleeve Open, Model No. 121414 and 121415. Product Usage: The product is intended to provide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Breg Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 16, 2014
Reusable latex breathing bags with multiple part numbers and sold as part of test lung part number and reusable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical, Inc.
FDA (openFDA device enforcement)
Reported Apr 16, 2014
Playtex Nurser Deluxe Double Electric Breast Pump, Model X06578AO, powered by a 12V DC power supply, Model SY-12120,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Energizer Personal Care
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.