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 Jul 1, 2015
Cambridge House Royal Smoked Salmon Sliced Side Products are packaged in Reduced Oxygen Package (ROP). Product is…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Santa Barbara Smokehouse, Inc.
8 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 1, 2015
Chocolate covered wafers (Bocadin) in plastic packaging sold under the Mi Costenita brand and packaged and distributed…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Yoli, Inc. dba Mi Costenita
FDA (openFDA food enforcement)
Reported Jun 24, 2015
Amerigel Hydrogel Gauze Dressing 2 x 2, A5002. Wound Management.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerx Health Care Corp.
FDA (openFDA device enforcement)
Reported Jun 24, 2015
BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon Light Glove Part Number: 584569 Ophthalmic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beaver-Visitec International Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 24, 2015
HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and 1103 / OUS: 1100,1101,1102,1104,1104JP and 1205.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2015
Navigation System II-Cart, 7700-100-000 with Articulated Arm Camera, 7700-103-001 and Articulated Arm Camera,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Jun 17, 2015
AGFA DX-D 100 is a mobile digital radiography x-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Healthcare Corp.
FDA (openFDA device enforcement)
Reported Jun 17, 2015
BBL Port A Cul tubes, catalog number 221606. Patient sample collection tubes. BBL Port A Cul tubes, jars and vials…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2015
Roscoe Mini Neb Compressor User Manual for the NEB-ROS Product Usage: Inhaler therapy that converts liquid medicine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Compass Health Brands
FDA (openFDA device enforcement)
Reported Jun 17, 2015
HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and 1103 / OUS: 1100, 1101,1102,1104,1104JP and 1205.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2015
Rugby Poly Vitamin Liquid, 50ml
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pharmatech LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 17, 2015
Low Volume Extension Set, 72' w/Clamp FLL/MLL APV=1.3ml, STERILE, AND FLUID PATH NONPYROGENIC UNLESS PACKAGE IS DAMAGED…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical Asd Inc.
FDA (openFDA device enforcement)
Reported Jun 10, 2015
Oncentra Brachy radiation therapy planning software designed to analyze and plan radiation treatments in three…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2015
Alere i Influenza A & B Product Usage: The Alere i Influenza A and B assay, performed on the Alere i Instrument, is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere Scarborough, Inc. dba Binax, Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2015
SMARTABLATE RF Generator System, Catalog No. M490006, M490007, M4900106, and M4900107. Product Usage: The use of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosense Webster, Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2015
EliteCore Full Core Biopsy Device. EliteCore 18G, 20cm with and without HiLiter tip, 15 cm with and without HiLiter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Jun 3, 2015
Sun Rich Apple Slices with Caramel Dip, Parfait Cup, 6 x 6 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sun Rich Fresh Foods Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 3, 2015
100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 27, 2015
ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip, Product Usage: The instruments have application in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported May 27, 2015
Mucolytic Agent 1 pint/473 ml; 1 gallon/3.8 l Product Usage: A mucoliquefying preservative designed for use in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richard-Allan Scientific Company
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 27, 2015
Homocysteine test system - Homocysteine Reagent. 05385415190; Homocysteine 100 Tests, cobas c, COBAS INTEGRA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported May 20, 2015
Terra Spice Company Jalapeno Cheddar (dry spice mix). Sold in 0.5, 1, 3, or 5 qt. jars, 6x10 stand up pouches, and bulk…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greenies LLC d.b.a. Terra Spice Company
5 more products in this recall
FDA (openFDA food enforcement)
Reported May 20, 2015
HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product Usage: Is intended to repair the driveline…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare Inc.
FDA (openFDA device enforcement)
Reported May 20, 2015
Bountiful Harvest Chopped Spinach, KEEP FROZEN, Net Wt. 3 LBS. (1.36kg), Case with 12; Chopped Spinach (Cheney…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Magic Valley Fresh Frozen, Inc.
FDA (openFDA food 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.