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. 2,634 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,634 in last 12 months

Showing 84018420 of 28,748 recalls

Medical DeviceFebruary 24, 2022· Boston Scientific Corporation

Recalled Item: SpaceOAR System Recalled by Boston Scientific Corporation Due to Users need...

The Issue: Users need to be aware that embolism is a possible adverse event associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee biplane Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen floor Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor MN Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q ceiling Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q zeego Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee multi-purpose Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee biplane MN Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q floor Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee ceiling Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen biplane Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q biplane Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen ceiling Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Carefusion 2200 Inc

Recalled Item: (a) CareFusion Snowden-Pencer Plastics Recalled by Carefusion 2200 Inc Due...

The Issue: The finished device package did not contain the IFU.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2022· Busse Hospital Disposables, Inc.

Recalled Item: SS 4.5MM Pellet Insertion Tray with Large Gloves Catalog Number: B1363...

The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2022· Busse Hospital Disposables, Inc.

Recalled Item: I.V. Start Kit - Tegaderm Dressing - Catheter Securement - Recalled by Busse...

The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2022· Busse Hospital Disposables, Inc.

Recalled Item: Sterile Epidural Tray Catalog Number: 6259R2 Recalled by Busse Hospital...

The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2022· Busse Hospital Disposables, Inc.

Recalled Item: SS 3.5Mm Pellet Insertion Tray with large Gloves Catalog Number: B1352R1...

The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...

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

Class II — Potential Health HazardOngoing