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 Mar 13, 2019

Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut…

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Mar 13, 2019

Comprehensive Reverse Shoulder System Glenosphere Mini Baseplate with Taper Adapter, Model Number 010000589 Biomet…

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

Zimmer Biomet, Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Mar 9, 2019

Conagra Brands, Inc. Recalls Chicken and Rice Products Due To Misbranding and Undeclared Allergens

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

Hometown Food Company

USDA FSIS

Medical devices

Reported Mar 6, 2019

Alcon or Endure Ophthalmic Microscope Product Usage: Used for low magnification visualization during ophthalmic…

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

Alcon Research Laboratories Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2019

Phoenix AST-s Indicator, Catalog Number 246009

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

Becton Dickinson & Co.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2019

Entuit Secure Gastrointestinal Suture Anchor Set, Catalog Number GIAS-SRM-2, Order Number G35569 The Entuit Secure…

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

Cook Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 6, 2019

Montmorency Tart Cherry Concentrate 100% Juice 32-oz bottle (sold individual and 12 per case), 16-oz bottle (sold…

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

King Orchards

FDA (openFDA food enforcement)

Medical devices

Reported Mar 6, 2019

The WinStation Retinal Imager, also known as Merge Eye Station. DCF-1024 & DCF-512 Digital Imaging System Product…

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

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 27, 2019

AMIA Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution…

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

Baxter Healthcare Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 27, 2019

Stingray" Guidewire, labeled as 300cm. intended to facilitate placement of balloon dilatation catheters or other…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 20, 2019

COBRA FUSION 50, Ablation System, Catalog # (REF) 700-002

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

AtriCure, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 20, 2019

Coconut Chocolate RXBARs , 1.83 oz., single bar, , 12-count carton, 5-count carton, 4-count carton

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

Chicago Bar Company LLC Rxbar

18 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 20, 2019

Hemotherm CE Dual Reservoir Cooler/Heater, Model No. 400CE Product Usage: The HEMOTHERM¿ Model 400CE Dual Reservoir…

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

Cincinnati Sub-Zero Products LLC, a Gentherm Company

FDA (openFDA device enforcement)

Food

Reported Feb 20, 2019

Culinary Secrets, Butterscotch Instant Pudding Mix, Net Wt. 28 OZ, Marketed by Independent Marketing Alliance, Houston,…

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

Diamond Crystal Brands, Inc.

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 20, 2019

MOSAIQ¿ Oncology Information System and Sequencer MOSAIQ is an oncology information system used to manage workflows for…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Feb 20, 2019

Clobetasol Propionate Topical Solution USP, 0.05% w/w, 50 mL bottle, Manufactured for: Macleods Pharma USA, Inc.…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Oxalis Labs

FDA (openFDA drug enforcement)

Food

Reported Feb 20, 2019

Parent's Choice Toddler Next Stage¿ Milk Drink Powder Natural Milk Flavor With Other Natural Flavors, Stage 3, 1 Year…

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

PBM Nutritionals, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 13, 2019

ARCHITECT Free T3 Reagent Kit used on ARCHITECT i1000SR or i2000/i2000SR platforms Product Usage: It is a…

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

Abbott Ireland Diagnostics Division

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2019

BARD SureStep Foley Tray System Bardex I.C. Complete Care Temperature Sensing Infection Control Foley Catheter with…

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

Bard Medical Division

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 13, 2019

Gold Medal Unbleached All Purpose Flour. Net Wt 5 lb. (2.26kg). UPC 16000-19610. Distributed By General Mills Sales,…

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

General Mills, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 13, 2019

Portex 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿

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

Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

12 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 13, 2019

Mrs GRISSOM'S SELECT OLD FASHIONED PIMENTO CHEESE**Mrs. GRISSOM'S SELECT CRANBERRY PECAN CHICKEN SALAD**INGREDIENTS:…

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

Mrs Grissom's Salads, Inc.

FDA (openFDA food enforcement)

Food

Reported Feb 13, 2019

Chicago's Pizza Base Mix, Manufactured Exclusively for Chicago's Pizza, Greenfield, IN packaged in 30 lb bags.

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

Pizza Blends, LLC

9 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 6, 2019

Peaches, sold as a bulk retail item, with PLU 4044, and country of origin of Chile. The peaches sold at Aldi are…

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

Jac Vandenberg Inc.

2 more products in this recall

FDA (openFDA food enforcement)

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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.