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. 2,639 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,639 in last 12 months

Showing 70617080 of 51,386 recalls

Medical DeviceDecember 26, 2023· Ossur H / F

Recalled Item: Power Knee Recalled by Ossur H / F Due to Knee batteries may need...

The Issue: Knee batteries may need replacement with conforming batteries to ensure...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2023· Onkos Surgical, Inc.

Recalled Item: ELEOS COLLAR STEM Recalled by Onkos Surgical, Inc. Due to Mislabeling

The Issue: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2023· Onkos Surgical, Inc.

Recalled Item: ELEOS COLLAR STEM Recalled by Onkos Surgical, Inc. Due to Mislabeling

The Issue: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Exactamix Pro 1200 Recalled by Baxter Healthcare Corporation Due to...

The Issue: An error was identified in software versions 2.0.8 and 2.1.8 while using the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Exactamix Pro 2400 Recalled by Baxter Healthcare Corporation Due to...

The Issue: An error was identified in software versions 2.0.8 and 2.1.8 while using the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2023· Howmedica Osteonics Corp.

Recalled Item: HRIS ACET CUP CUT TIP 26X140 Part Number: 6210-5-100. single-use Recalled by...

The Issue: Failed to meet the acceptance criteria for the seal integrity and/or package...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2023· Howmedica Osteonics Corp.

Recalled Item: HRIS ACET CUP CUT TIP 32X140 Part Number: 6210-5-200rker. single-use...

The Issue: Failed to meet the acceptance criteria for the seal integrity and/or package...

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

Class II — Potential Health HazardOngoing
FoodDecember 21, 2023· County Fair Foods, Inc.

Recalled Item: Popcorn Pre-Pop in 8oz Polypropylene bag packaged 20 bags to a case Recalled...

The Issue: Undeclared Yellow #5

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2023· Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company

Recalled Item: Americaine Recalled by Insight Pharmaceuticals LLC, a Prestige Consumer...

The Issue: Chemical Contamination: presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 21, 2023· PFIZER

Recalled Item: Bleomycin for Injection Recalled by PFIZER Due to Presence of particulate...

The Issue: Presence of particulate matter: glass

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 21, 2023· Pharma Nobis LLC

Recalled Item: Freskaro & revitalize Magnesium Citrate Saline Laxative Oral Solution...

The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2023· Pharma Nobis LLC

Recalled Item: Good Neighbor Pharmacy Recalled by Pharma Nobis LLC Due to MICROBIAL...

The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2023· Pfizer Inc.

Recalled Item: 4.2% Sodium Bicarbonate Injection Recalled by Pfizer Inc. Due to Presence of...

The Issue: Presence of Particulate Matter; identified as glass

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 21, 2023· Pharma Nobis LLC

Recalled Item: CVS Health Magnesium Citrate Saline Laxative Oral Solution DYE FREE Recalled...

The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2023· Pharma Nobis LLC

Recalled Item: Freskaro & revitalize Magnesium Citrate Saline Laxative Oral Solution...

The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2023· Pfizer Inc.

Recalled Item: 8.4 % Sodium Bicarbonate Injection Recalled by Pfizer Inc. Due to Presence...

The Issue: Presence of Particulate Matter; identified as glass

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 21, 2023· Pfizer Inc.

Recalled Item: Atropine Sulfate Injection Recalled by Pfizer Inc. Due to Presence of...

The Issue: Presence of Particulate Matter; identified as glass

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 21, 2023· Pharma Nobis LLC

Recalled Item: Walgreens Dye-Free Magnesium Citrate Saline Laxative/Oral Solution Recalled...

The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 21, 2023· AMD Medicom Inc.

Recalled Item: PATTERSON¿ PROCEDURE EARLOOP MASKS- ANTI-FOG Recalled by AMD Medicom Inc....

The Issue: Level 3 masks were produced on alternate non-validated production equipment...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2023· AMD Medicom Inc.

Recalled Item: HENRY SCHEIN¿ CRITERION¿ EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-2448)...

The Issue: Level 3 masks were produced on alternate non-validated production equipment...

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

Class II — Potential Health HazardOngoing