Product Recalls in Kentucky

Product recalls affecting Kentucky — including food, drugs, consumer products, medical devices, and vehicles distributed to Kentucky. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,049 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
1,049 in last 12 months

Showing 16641–16660 of 51,386 recalls

FoodFebruary 26, 2021· J & J Distributing Company

Recalled Item: Haug Fresh Mini 7 Layer Dip Tray Recalled by J & J Distributing Company Due...

The Issue: Products may be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 26, 2021· J & J Distributing Company

Recalled Item: tastebuds Taco Platter Recalled by J & J Distributing Company Due to...

The Issue: Products may be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 26, 2021· Laboratorios Pisa Sa De Cv

Recalled Item: Electrolit Fruit Punch Zero Recalled by Laboratorios Pisa Sa De Cv Due to...

The Issue: Product contains undeclared FD&C Red No. 40.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
DrugFebruary 26, 2021· Alvogen, Inc

Recalled Item: Buprenorphine and Naloxone Sublingual Film 2mg/0.5mg Recalled by Alvogen,...

The Issue: Subpotent drug: Out of specification for assay of naloxone and buprenorphine...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Progesterone Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed Dissolution Specifications: Out-of-specification results observed for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 25, 2021· Fenwal Inc

Recalled Item: Amicus Exchange Kit - Product Usage: intended for use in Recalled by Fenwal...

The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Fenwal Inc

Recalled Item: Amicus MNC Apheresis Kit - Double Needle - Product Usage: Recalled by Fenwal...

The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Tenacore LLC

Recalled Item: Alaris Infusion Pump 8100 Bezel (plastic piece only) Recalled by Tenacore...

The Issue: Bezel repair parts used, not by the original manufacturer, to service and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: In-View Clear Leggings Bulk Non-Sterile Recalled by Cardinal Health 200, LLC...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Tenacore LLC

Recalled Item: Alaris Infusion Pump Module Recalled by Tenacore LLC Due to Bezel repair...

The Issue: Bezel repair parts used, not by the original manufacturer, to service and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: Femoral Angiography Drape Bulk Non-Sterile Recalled by Cardinal Health 200,...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: Femoral Angiography Drape Sterile Recalled by Cardinal Health 200, LLC Due...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Fenwal Inc

Recalled Item: Amicus Exchange Kit Therapeutics - Product Usage: intended for use Recalled...

The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· BioMedical Equipment Service Co (BMES)

Recalled Item: Alaris Infusion Pump Module Recalled by BioMedical Equipment Service Co...

The Issue: Bezel repair parts used, not by the original manufacturer, to service and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: In-View Clear Leggings Sterile Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: In-View Clear Leggings Sterile Non-Sterile Recalled by Cardinal Health 200,...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2021· Arthrex, Inc.

Recalled Item: Drill Bit Recalled by Arthrex, Inc. Due to The color indicator on the...

The Issue: The color indicator on the proximal end of the shaft of the AR-8770-02 is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2021· Philips Healthcare (Suzhou) Co., Ltd.

Recalled Item: Philips CT systems are advanced continuous-rotation computed tomography...

The Issue: Philips has internally detected an issue with the actuators used in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2021· Trinity Sterile, Inc.

Recalled Item: Midline Catheter Dressing Change Kit with Statlock - Product Usage: Recalled...

The Issue: Evidence of face masks or other material in the seal in several kits,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Mindray BeneVision Distributed Monitoring System( DMS) 1. p/n 115-051209-00...

The Issue: BeneVision DMS may intermittently freeze and require a manual reboot after...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing