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 2, 2018
EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM, Product Number HEM3335, GTIN Number 1 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 2, 2018
Versatex Monofilament Mesh 50 x 50cm, Product No. VTX5050M The device is made out of a macroporous three-dimensional…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sofradim Production
FDA (openFDA device enforcement)
Reported May 2, 2018
Flowmeter Module (accessory to Terumo Advanced Perfusion System 1). Provides the interface between the flow sensor and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Apr 25, 2018
Kratom capsules labeled in the following ways: 1) Divinity Kratom 10 Capsule Dietary Supplement, Divinity Product LLC,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Divinity Product Distribution LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 25, 2018
Midwest Northern Nut Roasted Salted Natural Almonds. Packaged in the following sizes: 1. Net Wt. 16 oz. (454G), UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Midwest Northern Inc.
65 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 25, 2018
Cali Green Malay Kratom all packages, all quantities
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nutrizone LLC
9 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 25, 2018
Chicken bacon, egg white and cheese on flat bread sandwich
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Premier Food Management, LLC
FDA (openFDA food enforcement)
Reported Apr 25, 2018
MEVATRON M2 / PRIMUS Mid-Energy, Digital Linear Accelerator, Model No. 01940035 Product Usage: The intended use of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 25, 2018
Zimmer Segmental System Proximal Femoral Component 38mm Offset, Model Number 00-5850-030-38 The Segmental System is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Apr 18, 2018
First aid/emergency kits containing Honeywell eyewash: CSM kit number Kit/cabinet Description CSM Eyewash# Size:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Certified Safety Mfg Inc.
FDA (openFDA device enforcement)
Reported Apr 18, 2018
VOLISTA StandOP Surgical Light; Model numbers VLT600 SF AIM STP, VLT600 DF AIM STP, Ref. codes ARD568811901,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge US Sales LLC
FDA (openFDA device enforcement)
Reported Apr 18, 2018
Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults and pediatrics and optionally infants and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hamilton Medical AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 11, 2018
HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 11, 2018
King Arthur Flour, 100% Organic, Finely Ground, Coconut Flour, UPC 0 71012 10702 5, Distributed by: The King Arthur…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The King Arthur Flour Company, Inc.
FDA (openFDA food enforcement)
Reported Apr 7, 2018
J.T.M. Provisions Company Retira De Productos De Carne De Res Debido A Una Posible Contaminacin Con Materia Externa
Moderate riskThis product could cause temporary or reversible health problems — stop using it.J.T.M. Provisions Company
USDA FSIS
Reported Apr 4, 2018
Rechargeable Li-ion battery used with Puritan Bennett TM 980 Series Ventilator System including Pediatric-Adult…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 4, 2018
(1) Sigma HP Cemented Trochlea Size 1 Narrow Left, Catalog Number: 102403100, GTIN: 10603295001614; (2) Sigma HP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A7AP, UDI: 04560141940031
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Konica Minolta Medical Imaging USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Gas Module 3 monitoring spirometer, Part Number: 115-030108-00 Product Usage: The Gas Module 3 is an accessory device…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Sour Patch Kids, 1.9 lb bag
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mondelez Global LLC
FDA (openFDA food enforcement)
Reported Mar 28, 2018
BD Vacutainer¿ EDTA Lavender Top Tubes: Catalog Numbers: 1. 366401 (UDI: 50382903664011); 2. 366450 (UDI:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Becton Dickinson & Company
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 28, 2018
Malecot Nephrostomy Catheter System, Product Number: M001224110, GTIN: 08714729030980 The Malecot and the Stenting…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 28, 2018
ClariVein IC infusion catheter, Model Number: 65-018-E4S Product Usage: The ClariVein IC infusion catheter is indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascular Insights, LLC
FDA (openFDA device enforcement)
Reported Mar 21, 2018
NovaKone Daily Wear Soft contact; Catalog Number: AONKS54 Product Usage: The NOVAKONE SPHERICAL lens is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alden Optical
10 more products 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.