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. 1,841 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
1,841 in last 12 months

Showing 3004130060 of 51,386 recalls

DrugMay 17, 2017· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Presence of an impurity peak...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 17, 2017· Biosense Webster, Inc.

Recalled Item: PENTARAY NAV High-Density Mapping Catheter. Recalled by Biosense Webster,...

The Issue: Contraindication language updated in the Instructions For Use (IFU) to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2017· Biosense Webster, Inc.

Recalled Item: PENTARAY NAV High-Density Mapping Catheter. Recalled by Biosense Webster,...

The Issue: Contraindication language updated in the Instructions For Use (IFU) to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2017· Z-Medica, LLC

Recalled Item: QuikClot TraumaPad Recalled by Z-Medica, LLC Due to Packaging breach may...

The Issue: Packaging breach may compromise sterility

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

Class II — Potential Health HazardOngoing
DrugMay 16, 2017· Lupin Limited (Unit 1)

Recalled Item: Mibelas 24 Fe (Norethindrone acetate and Ethinyl estradiol 1 mg/0.02...

The Issue: Contraceptive Tablets Out of Sequence- First 4 pills of the packet are...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 16, 2017· GlaxoSmithKline, LLC

Recalled Item: Ventolin HFA (albuterol sulfate) Inhalation Recalled by GlaxoSmithKline, LLC...

The Issue: Defective Delivery System: Elevated number of units with out of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 15, 2017· Beckman Coulter Inc

Recalled Item: Beckman Coulter Synchron AQUA CAL Level 1 Recalled by Beckman Coulter Inc...

The Issue: The firm identified a negative shift of 5mmol/L for sodium recovery in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2017· Perkinelmer Life Sciences, Inc.

Recalled Item: Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06...

The Issue: Potential for electric shock in the case of a failure to install the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2017· Smiths Medical ASD Inc.

Recalled Item: CADD¿ High Volume Administration Set with FlowStop Recalled by Smiths...

The Issue: One lot of CADD¿ High Volume Administration sets, part number 21-7381-24,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2017· Mesa Laboratories, Inc.

Recalled Item: MesaLabs Conductivity Standard Solution Recalled by Mesa Laboratories, Inc....

The Issue: Mesa Laboratories is recalling Conductivity/TDS Calibrator Solution due to...

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

Class II — Potential Health HazardOngoing
FoodMay 11, 2017· Global Garlic, Inc.

Recalled Item: Queso Fresco x LB (Barra)/ Whole Milk Cheese Recalled by Global Garlic, Inc....

The Issue: Product contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 11, 2017· Global Garlic, Inc.

Recalled Item: De Mi Pais Recalled by Global Garlic, Inc. Due to Potential Listeria...

The Issue: Product contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 11, 2017· Lamb Weston Inc

Recalled Item: Red Robin Burgers and Brews Crispy Onion Rings Recalled by Lamb Weston Inc...

The Issue: Red Robin Burgers and Brews Crispy Onion Rings, 14 oz. retail packages, are...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 11, 2017· Tyson Foods, inc.

Recalled Item: Chef Pierre 10 Spinach Quiche Recalled by Tyson Foods, inc. Due to Potential...

The Issue: The firm is voluntarily recalling multiple lots of frozen Chef Pierre 10...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 11, 2017· Tyson Foods, inc.

Recalled Item: Sara Lee CP Quiche 10 Spinach Recalled by Tyson Foods, inc. Due to Potential...

The Issue: The firm is voluntarily recalling multiple lots of frozen Chef Pierre 10...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Optima MR450 1.5T Product Usage: 1 .5T Brivo MR355 and Recalled by GE...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Optima MR750 3.0T Product Usage: The Optima MR450 1.5T system Recalled by GE...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Optima MR450w 1.5T Product Usage: The Optima MR450w 1.5T system Recalled by...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: 1.5T Signa HDxt Recalled by GE Medical Systems, LLC Due to Possible...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: 1.5T Signa HDx Recalled by GE Medical Systems, LLC Due to Possible incorrect...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing