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 Oct 31, 2018

Boston Scientific Maestro 4000 Cardiac Ablation System, Firmware Version 5.14, Model Numbers: M00440000, M0044000D0,…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Food

Reported Oct 31, 2018

Callie's Charleston Biscuits COCKTAIL HAM BISCUITS; 24 NET WT. 35 OZ (980 g) Callie's Charleston Biscuits; 1895 Avenue…

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

Callie's Charleston Biscuits

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 31, 2018

Cedar's Chickpea Salad, packaged in an 8oz plastic container, UPC: 044115337767. Product is refrigerated.

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

Cedar's Mediterranean Foods, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 31, 2018

CHS Custom Convenience Kit-DR. NANDA CLOSING TRAY(CONMED HYFRECATOR SHARP) Product Number: B9-15934B

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

Custom Healthcare Systems, Inc.

28 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2018

Mitek Screw and Washer Depth Gauge, Product Code 219024

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

DePuy Mitek, Inc., a Johnson & Johnson Co.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2018

Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the…

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

Ecolab Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2018

O-arm 1000 2nd Edition Imaging System, OARM ASSY Bl70000027 SYSTEM PRODUCT, Model Number Bl70000027 Product Usage: The…

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

Medtronic Navigation, Inc.-Littleton

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2018

APTIO INPUT/OUTPUT MODULE

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

Siemens Healthcare Diagnostics, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 24, 2018

CAFFEINE FREE Diet Coke 12 FL OZ (355 ml) CONTAINS PHENYLALANINE CAFFEINE FREE THE COCA-COLA COMPANY FOR CONSUMER…

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

Coca Cola Bottling Compan

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 24, 2018

GE Healthcare MRI Systems, Software Version 11.x, sold under the following product names: 1.5T CXK4 LCC MAGNET,1.5T…

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

GE Medical Systems, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 24, 2018

La Mexicana Hot Salsa 16 oz., 24 oz., 48 oz., 64 oz., and 128 oz. Gourmet Style Hot Salsa 16 oz.

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

La Mexicana LLC

6 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 24, 2018

Terumo¿ Advanced Perfusion System 1 Electronic Patient Gas System, Catalog#: 801188

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

Terumo Cardiovascular Systems Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 24, 2018

Thoratec CentriMag Motor, Model: 102956, a component of the Thoratec CentriMag Blood Pumping System and PediMag Blood…

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

Thoratec Switzerland GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Oct 24, 2018

Affixus Hip Fracture Nail 125 9 mm x 180 mm, Item Number 814309180 Product Usage: Intended for the fixation of fractures

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

Zimmer Biomet, Inc.

47 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 17, 2018

Colpo-Pneumo Occluder, Part CPO-6

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 17, 2018

Lic's REESE'S OREO, ONE QUART (946 mL), packed in Plastic quart container

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

Lloyd'S Ice Cream Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 17, 2018

NeoMed Enteral Feeding Tubes with Enteral Only Connectors, French sizes 4.0Fr, 5.0Fr, 6.5Fr, 8.0Fr, and lengths 40cm,…

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

Neomed Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 17, 2018

Miso Milo Chocolate (cookies); A Sarap Asian Fusion Product; Net Wt. 70 G/Cookie; Contains: Flour, eggs, Baking Soda,…

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

Sarap Asian Fusion

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 10, 2018

ENDOLOGIX AFX Endovascular AAA System, Stent Graft System, Rx Only, Sterile EO, REF: BA22-120/I20-40, BA22-100/I20-40,…

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

Endologix

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 10, 2018

Meijer Taco Seasoning Mix, Net wt. 4.5 oz.

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

McCormick & Company, Inc. - Flavor Manufacturing Center

FDA (openFDA food enforcement)

Food

Reported Oct 10, 2018

Crazy About Cookies***GLUTEN FREE CHOCOLATE CHIP COOKIE DOUGH**Net Wt. 2 lbs. (907.18g)**Nutrition facts***Ingredients:…

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

Neighbors LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 10, 2018

TrueBeam Radiotherapy Delivery System version 2.0 and 2.5 EDGE Radiotherapy Delivery System version 2.0 and 2.5 Product…

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

Varian Medical Systems

1 more product in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Oct 5, 2018

Ukrop's Homestyle Foods Retira Productos De Carne Y Avicultura Listos Para El Consumo Por La Posible Contaminacin…

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

Ukrop's Homestyle Foods

USDA FSIS

Medical devices

Reported Oct 3, 2018

Bausch + Lomb Stellaris Elite 20 GA Vit Cutter, Model BL5626, 7500 cpm, packaged in sterile pouches, 6/shipper.

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

Bausch & Lomb Inc.

12 more products in this recall

FDA (openFDA device 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.