All recall categories

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.

Medical devices

Reported Sep 25, 2019

Hemospray Endoscopic Hemostat

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Wilson-Cook Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 18, 2019

Natrelle, Saline-Filled Breast Implant Biocell Full Height with Fill Tube, Sterile, for the following style numbers:…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Allergan PLC

14 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 18, 2019

YoCrunch VANILLA LOWFAT YOGURT WITH SNICKERS PIECES 4 - 4 oz (113g) - 16 oz (453g) 6 packaged or 4 cups per case. UPC…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Danone Waters

FDA (openFDA food enforcement)

Food

Reported Sep 18, 2019

PediaSmart Organic Soy Vanilla Beverage Mix, 12.7 oz. (360g) composite can

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Natures One Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 18, 2019

Dynex DSX Software-IVD ELISA Assays effected as follows: DSX Assay File Software: ZEUS vl B. burgdorferi lgG-lgM.asy…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zeus Scientific, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 18, 2019

XP- CR Tibial Tray- Interlok 59mm Item # 195268

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer Biomet, Inc.

34 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2019

Alere Cholestech LDX Analyzer, model # 14-874 containing power supplies with the identifying codes of 1837d and 1843d -…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alere San Diego, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2019

Alaris EtCO2, Model 8300, UDI: 10885403830013, CareFusion for models 11634567 and 8300ADXeN933

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2019

Norm-O-Temp model 111Z

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cincinnati Sub-Zero Products LLC, a Gentherm Company

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2019

EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product Code:5905190, 14.5 Fr. Alphacurve Catheter with Standard Kit,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Peripheral Vascular Inc.

27 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 4, 2019

All colors and sizes of Confectionery Arts International, LLC brand Jewel Dust, a pearlescent pigment, manufactured and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Confectionery Arts International, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 4, 2019

Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is fully integrated and automated instrument including…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Phadia Ab

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2019

Roche Elecsys Anti-CCP Immunoassay Catalog # 07251670190

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Roche Diagnostics Operations, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2019

Kit BD Max Check-Points CPO IVD EU; Catalog # 278102

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Co.

18 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2019

DeRoyal Enteral Safe Feeding Tubes: a) REF 54-2450R, 5 FR x 24" Polyurethane b) REF 54-2465R, 6.5 FR x 24" Polyurethane…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

DeRoyal Industries Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 28, 2019

Dole Baby Spinach: 6 oz. (170 g) plastic bag, UPC 0-71430-00964-2, SKU 320; 10 oz. (283 g) clamshell, UPC…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Dole Fresh Vegetables Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 28, 2019

ABL90 FLEX Analyzer REF 393090 UDI:05700693930909

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2019

ACUSON NX2 Diagnostic Ultrasound System, Model # 11284381, RX Only, Siemens Medical Solutions, containing software…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2019

MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 28, 2019

PRIVATE SELECTION FROZEN TRIPLE BERRY MEDLEY, 48 oz

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)

Drugs

Reported Aug 28, 2019

Bexarotene Capsules, 75 mg, 100 capsules per bottle, Rx Only, Manufactured for: Upsher-Smith Laboratories, LLC, Maple…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Upsher Smith Laboratories, Inc.

FDA (openFDA drug enforcement)

Food

Reported Aug 21, 2019

Entenmann's Little Bites Soft Baked Cookies (5 pack Mini Chocolate Chip variety) Net Weight of 5ct box 6.88oz. 5…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BIMBO Bakeries USA Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 21, 2019

iGUIDE System with software build iGuide 2.2.0, 2.2.1, and 2.2.2

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Elekta, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 21, 2019

Freshness Guaranteed Chocolate Chunk cookie Clear plastic clam shell Net wt. 14 oz. UPC: 0007874209234

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hill & Valley Inc.

FDA (openFDA food enforcement)

Free recall alerts

Get alerted about new Kentucky recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Other states

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.