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. 2,672 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,672 in last 12 months

Showing 22412260 of 51,386 recalls

Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Intera 1.5T Achieva Nova Product Number: 781172 Recalled by Philips North...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Intera Achieva 1.5T Pulsar Recalled by Philips North America Due to...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Intera 1.5T Master/Nova Product Number: 781106 Recalled by Philips North...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Intera 1.5T Omni/Stellar Recalled by Philips North America Due to identified...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Achieva XR Product Numbers: (1) 781153 Recalled by Philips North America Due...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

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

Class II — Potential Health HazardOngoing
DrugMay 28, 2025· Apotex Corp.

Recalled Item: Ketorolac Tromethamine Ophthalmic Solution Recalled by Apotex Corp. Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2025· Apotex Corp.

Recalled Item: Azelastine HCl Ophthalmic Solution Recalled by Apotex Corp. Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2025· Pfizer Inc.

Recalled Item: DOBUTamine Injection Recalled by Pfizer Inc. Due to Discoloration;...

The Issue: Discoloration; discolored solution from cracked vials

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2025· Apotex Corp.

Recalled Item: Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution Recalled by Apotex...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2025· Apotex Corp.

Recalled Item: Lacosamide Oral Solution Recalled by Apotex Corp. Due to Defective...

The Issue: Defective Container: This recall is being initiated due to a leaking unit...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips eL18-4 EMT Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips C9-5EC Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips eL18-4 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips C5-2 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips L12-3 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips X6-1 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips X8-2t Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips V6-2 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips S5-1 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips S7-2 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing