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 Jun 6, 2018
SOMATOM go.Now, Material Number 11061618 There is a potential for a software issue that may cause the need for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 6, 2018
LINX Reflux Management System, Implant Suture, 12-17 Bead, 0.7T, Product Code LS-xx, sterile, Rx only. Labeled as: a.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Torax Medical, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 6, 2018
Ziyad Brand Tahini, 8oz, 16oz, ¿ gal, 32oz. , packed in glass jars
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ziyad Brothers Importing, Inc.
FDA (openFDA food enforcement)
Reported May 30, 2018
Edwards Lifesciences' IntraClude Intra-Aortic Occlusion Device. Packaged in a sterile barrier system. Model Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported May 30, 2018
Southwestern Gourmet Butter Popcorn Grand Canyon Foods, Phoenix, AZ
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Grand Canyon Foods International LLC.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 30, 2018
ImplantDirect simply InterActive Implant, 5.0mmD X 10mmL, SBM: 3.4mmD Platform, Part #655010U, Rx, Sterile. Incorrect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 30, 2018
Sorin Stockert Heater-Cooler System 3T, a) Item #: 16-02-81, 240 v/60 Hz; b) Item #: 16-02-82, 208 v/60 Hz; c) Item #:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 30, 2018
First Step Endoscopic Cleaning Pad, 100ml, Flexible Endoscope Bedside Pre-Clean Kit, Catalogue Number EP-3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Madison Polymeric Engineering
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 30, 2018
Synthes Torque Limiting Handle, Part Number 03.231.013 This device is used in systems indicated for fracture fixation.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported May 23, 2018
Thoratec HeartMate 3 LVAS Implant Kit, Rx Only, Catalog # 106524US, 106524, 10652INT - LVAS KIT, HM 3 Indicated for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abbott
FDA (openFDA device enforcement)
Reported May 23, 2018
DIABEATIC Chocolate Berry Crunch bar NET WT 1.4 oz (42g)Manufactured and Distributed by eBars, LLC, Franklin, TN 37064…
High riskUsing this product could cause serious injury, illness or death — stop using it now.eBars
12 more products in this recall
FDA (openFDA food enforcement)
Reported May 23, 2018
Tosoh ST AIA-PACK HbA1c, HbA1c Reagent, Pt. No. 025218 The device is designed for In Vitro Diagnostic Use Only for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 23, 2018
Persona Stemmed Tibial Provisional Size H Left, Item Number 42532108301 For use during orthopaedic surgery for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 16, 2018
ARCHITECT DHEA-S Reagent Product Usage: It is a chemiluminescent microparticle immunoassay (CMIA) for the quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
FDA (openFDA device enforcement)
Reported May 16, 2018
MicroVue BAP EIA, Model 8012, provides a quantitative measure of bone-specific alkaline phosphatase (BAP) activity in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostic Hybrids, Inc.
FDA (openFDA device enforcement)
Reported May 16, 2018
NeoBase Succinylacetone Assay Solution, Product Number: 3042-0020; Affected UDI Numbers:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PerkinElmer Life and Analytical Sciences, Wallac, OY
FDA (openFDA device enforcement)
Reported May 16, 2018
ACUSON SC2000 Ultrasound System. The firm name on the label is Siemens Medical Solutions USA, Inc., Buffalo Grove, IL.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported May 9, 2018
Miriam Capsule Endoscope System. Model MR1100 Product Usage: MiroCam Capsule Endoscope System is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.IntroMedic Co., Ltd.
FDA (openFDA device enforcement)
Reported May 9, 2018
Happy Harvest Leaf Spinach; Net Wt. 13.5 oz (383g); Ingredients: Spinach, Water, Salt. Distributed by Aldi Inc.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mccall Farms Inc.
FDA (openFDA food enforcement)
Reported May 9, 2018
Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Interventional fluoroscopic x-ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported May 9, 2018
PTS Panels¿ CHOL+GLU Test Strips (REF 1765)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Polymer Technology Systems, Inc.
FDA (openFDA device enforcement)
Reported May 9, 2018
Modular Head Component, Biomet Hip System; Item No. 163669, Hip Joint, metal/polymer semi-constrained cemented…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 2, 2018
Advance¿ 35LP Low-Profile PTA Balloon Dilatation Catheter; Catalog numbers: PTA5-35-135-6-2 .0 and PTA5-35-135-4-4 .0;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
FDA (openFDA device enforcement)
Reported May 2, 2018
clariti 1 day/Fresh Day 90 pack (-1.00), UV Blocking, 90 silicon hydrogel, daily disposable contact lenses The Clariti…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.CooperVision Inc.
3 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.