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. 1,069 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
1,069 in last 12 months

Showing 16001–16020 of 51,386 recalls

Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic CB10W65R1 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY10D90R2 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic BB7D76R13 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY10J00R12 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY11B40R1 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY10Y54R4 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Covidien, LP

Recalled Item: HME for Tracheostomized Patients Recalled by Covidien, LP Due to The company...

The Issue: The company was notified by their supplier of sterilization services for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic CB10R55R5 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic 1A46R11 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY7M07R6 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic CB1H18R20 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY8M63R4 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY8R62R13 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
DrugApril 29, 2021· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 120 Thyroid Tablets Recalled by Acella Pharmaceuticals, LLC Due...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2021· Ascend Laboratories LLC

Recalled Item: Olmesartan Medoxomil Tablets Recalled by Ascend Laboratories LLC Due to...

The Issue: Presence of Foreign Tablet/Capsule

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

Class III — Low RiskOngoing
Refund
DrugApril 29, 2021· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 30 Thyroid Tablets Recalled by Acella Pharmaceuticals, LLC Due to...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2021· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 15 Thyroid Tablets Recalled by Acella Pharmaceuticals, LLC Due to...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2021· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 90 Thyroid Tablets Recalled by Acella Pharmaceuticals, LLC Due to...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2021· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 60 Thyroid Tablets Recalled by Acella Pharmaceuticals, LLC Due to...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2021· Lupin Pharmaceuticals Inc.

Recalled Item: Cefixime for Oral Suspension USP 100 mg/5mL Recalled by Lupin...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund