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. 1,897 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
1,897 in last 12 months

Showing 1722117240 of 51,386 recalls

Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 5.5"x10" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS PST Meters- IVD (Patient Self-Testing) measures blood-clotting...

The Issue: Possible Misinterpretation of Displayed Measuring Units from INR to %Quick...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS Prof (Professional) Meters- IVD professional healthcare...

The Issue: Possible Misinterpretation of Displayed Measuring Units from INR to %Quick...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 4"x11" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 5"x15" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 8"x16" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temperature Tubing 3"x100'. One roll per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temperature Tubing 4"x100'. One roll per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Beckman Coulter Inc.

Recalled Item: MicroScan Pos MIC Panel Type 34 - Product Usage: For Recalled by Beckman...

The Issue: Due to a customer report and internal investigation, it was confirmed that a...

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

Class II — Potential Health HazardOngoing
FoodDecember 1, 2020· Meijer Distribution

Recalled Item: True Goodness by Meijer Organic Green Peas Frozen 10 Oz Recalled by Meijer...

The Issue: Product may contain nightshade

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x10mm...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm Recalled...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 20mm Recalled...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 20mm x10mm...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm Recalled...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x15mm...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Biomet, Inc.

Recalled Item: Vanguard 360 Revision System Posterior Augment With Bolt - Product Recalled...

The Issue: Incorrect bolt -tibial bolts in package instead of femoral bolts may delay...

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

Class II — Potential Health HazardOngoing
DrugNovember 30, 2020· Advanced Nutriceuticals, LLC

Recalled Item: LL-37 Recalled by Advanced Nutriceuticals, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: due to concerns with production processes...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 30, 2020· Advanced Nutriceuticals, LLC

Recalled Item: AOD-9604 Recalled by Advanced Nutriceuticals, LLC Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: due to concerns with production processes...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 30, 2020· Advanced Nutriceuticals, LLC

Recalled Item: CEREBROLYSIN Recalled by Advanced Nutriceuticals, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility: due to concerns with production processes...

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

Class II — Potential Health HazardOngoing
Refund