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. 2,656 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,656 in last 12 months

Showing 39013920 of 28,748 recalls

Medical DeviceMay 10, 2024· Medtronic Neuromodulation

Recalled Item: Medtronic Ascenda Intrathecal Catheter Recalled by Medtronic Neuromodulation...

The Issue: Design update to the Ascenda Intrathecal Catheter Models 8780, 8781, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Canon Medical System, USA, INC.

Recalled Item: MRI systems: Vantage Orian MRT-1550 (MEXL-1550) Recalled by Canon Medical...

The Issue: The terminal block used to secure the power supply cable for the gradient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ethicon, Inc.

Recalled Item: PDS Plus Antibacterial (polydioxanone) Suture - Intended for use in Recalled...

The Issue: Issue on a specific packaging machine resulted in a hole in the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ethicon, Inc.

Recalled Item: MONOCRYL (poliglecaprone 25) Suture - Intended for use in general Recalled...

The Issue: Issue on a specific packaging machine resulted in a hole in the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ethicon, Inc.

Recalled Item: VICRYL (polyglactin 910) Suture - Indicated for use in general Recalled by...

The Issue: Issue on a specific packaging machine resulted in a hole in the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ethicon, Inc.

Recalled Item: PDS II (polydioxanone) Suture - Intended for use in general Recalled by...

The Issue: Issue on a specific packaging machine resulted in a hole in the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ethicon, Inc.

Recalled Item: VICRYL Plus Antibacterial (polyglactin 910) Suture - Indicated for use...

The Issue: Issue on a specific packaging machine resulted in a hole in the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Beaver Visitec International, Inc.

Recalled Item: Xstar Safety Slit Knife Recalled by Beaver Visitec International, Inc. Due...

The Issue: The wrong configuration of the blade was in the package. The bevel was on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ethicon, Inc.

Recalled Item: MONOCRYL Plus Antibacterial (poliglecaprone 25) Suture - Intended for use...

The Issue: Issue on a specific packaging machine resulted in a hole in the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Beaver Visitec International, Inc.

Recalled Item: Xstar Safety Slit Knife Recalled by Beaver Visitec International, Inc. Due...

The Issue: The wrong configuration of the blade was in the package. The bevel was on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ion Beam Applications S.A.

Recalled Item: IBA Proton Therapy System - PROTEUS 235 - Designed to Recalled by Ion Beam...

The Issue: Irradiation is not interrupted when some C230 Accelerator Control Unit...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with Eccentric Tips labeled as: 1) SOL-M 10ml Eccentric Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with Luer Slip Tips labeled as: 1) SOL-M 1ml Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with Low Dead Space labeled as: a) SOL-M 1ml Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with exchangeable needles labeled as: SOL-CARE: 1) SOL-CARE 10ml...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with Fixed Needles labeled as: a) SOL-M: 1) SOL-M Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringe Tip Caps labeled as: 1) SOL-M Syringe Tip Cap Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Echonous Inc

Recalled Item: Kosmos on iOS impacting iOS Recalled by Echonous Inc Due to Ultrasound...

The Issue: Ultrasound system has a bug in affected iOS software, which after DICOM...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· First Source Inc

Recalled Item: First Source Vision M. Portable cart and platform that supports Recalled by...

The Issue: Potential for the bolt that secures the positioning arm to the gas spring to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· First Source Inc

Recalled Item: First Source iQ Flex M. Portable cart and platform that Recalled by First...

The Issue: Potential for the bolt that secures the positioning arm to the gas spring to...

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

Class II — Potential Health HazardOngoing