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. 979 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
979 in last 12 months

Showing 37881–37900 of 51,386 recalls

Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Fenestrated Bipolar Forceps Recalled by Intuitive Surgical, Inc. Due to In...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Maryland Bipolar Forceps Recalled by Intuitive Surgical, Inc. Due to In...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Crocodile Grasper Recalled by Intuitive Surgical, Inc. Due to In certain...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Curved Needle Driver Recalled by Intuitive Surgical, Inc. Due to In certain...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Needle Driver Recalled by Intuitive Surgical, Inc. Due to In certain...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Fundus Grasper Recalled by Intuitive Surgical, Inc. Due to In certain...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Medium -Large Clip Applier Recalled by Intuitive Surgical, Inc. Due to In...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Cadiere Forceps Recalled by Intuitive Surgical, Inc. Due to In certain...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Maryland Dissector Recalled by Intuitive Surgical, Inc. Due to In certain...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2015· Carestream Health Inc

Recalled Item: CARESTREAM DRX-EVOLUTION X-Ray System Product Usage: The device is a...

The Issue: Software defect that impacts image alignment when using the automatic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2015· International Biophysics Corp.

Recalled Item: IBC Aortic Punch Catalog Numbers APM40 Recalled by International Biophysics...

The Issue: It was discovered that the heat seal placed onto sterile pouches may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2015· International Biophysics Corp.

Recalled Item: IBC Suction Wand Catalog Number 1990S Product Usage: The IBC Recalled by...

The Issue: It was discovered that the heat seal placed onto sterile pouches may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2015· International Biophysics Corp.

Recalled Item: IBC Vascular Loop Catalog Number CH111 Recalled by International Biophysics...

The Issue: It was discovered that the heat seal placed onto sterile pouches may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2015· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI 500 Blood Parameter Monitoring System. Provides continuous Recalled by...

The Issue: Inaccuracies in SvO2, temperature, pH, pCO2, pO2, Hematocrit, and Potassium...

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

Class II — Potential Health HazardOngoing
FoodAugust 7, 2015· PIAZZA PRODUCE, INC.

Recalled Item: BBQ Spice Recalled by PIAZZA PRODUCE, INC. Due to Product labeling does not...

The Issue: Product labeling does not contain a listing of ingredients.

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

Class III — Low RiskOngoing
Refund
FoodAugust 7, 2015· PIAZZA PRODUCE, INC.

Recalled Item: Taco seasoning Recalled by PIAZZA PRODUCE, INC. Due to Product labeling does...

The Issue: Product labeling does not contain a listing of ingredients.

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

Class III — Low RiskOngoing
Refund
FoodAugust 7, 2015· PIAZZA PRODUCE, INC.

Recalled Item: Lemon Pepper Recalled by PIAZZA PRODUCE, INC. Due to Undeclared Soybean

The Issue: Product labeling does not contain a listing of ingredients. Undeclared...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 7, 2015· PIAZZA PRODUCE, INC.

Recalled Item: Quebec Steak seasoning Recalled by PIAZZA PRODUCE, INC. Due to Undeclared...

The Issue: Product labeling does not contain a listing of ingredients. Undeclared...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 7, 2015· PIAZZA PRODUCE, INC.

Recalled Item: Onion salt Recalled by PIAZZA PRODUCE, INC. Due to Product labeling does not...

The Issue: Product labeling does not contain a listing of ingredients.

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

Class III — Low RiskOngoing
Refund
FoodAugust 7, 2015· PIAZZA PRODUCE, INC.

Recalled Item: Italian Herb seasoning Recalled by PIAZZA PRODUCE, INC. Due to Undeclared...

The Issue: Product labeling does not contain a listing of ingredients. Undeclared...

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

Class II — Potential Health HazardOngoing
Refund