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 40014020 of 51,386 recalls

DrugOctober 22, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Morphine Sulfate Extended-Release Tablets 15 mg Recalled by Dr. Reddy's...

The Issue: Failed Impurities/Degradation Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Morphine Sulfate Extended-Release Tablets 30 mg Recalled by Dr. Reddy's...

The Issue: Failed Impurities/Degradation Specification

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 22, 2024· ICU Medical, Inc.

Recalled Item: Allegedly counterfeit batteries manufactured by CSB batteries being used...

The Issue: ICU Medical has received reports of allegedly counterfeit CSB batteries...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica¿ CH ¿2-Microglobulin (B2M) - In vitro diagnostic use in Recalled by...

The Issue: Potential for falsely depressed auto-diluted results for samples above the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp EX Short...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Atellica CH Reaction Ring Cuvette Segment-has cuvettes that contain...

The Issue: A manufacturing defect causes Atellica CH Reaction Ring Cuvette Segments...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2024· Biomet, Inc.

Recalled Item: JuggerLoc/ToggleLoc 2.9mm Drill Guide Recalled by Biomet, Inc. Due to Firm...

The Issue: Firm received complaints reporting that guides were warped when pulled out...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Karl Storz Endoscopy

Recalled Item: Irrigation Tubing for KARL STORZ Endomat Select UP210 Recalled by Karl Storz...

The Issue: Due to improper labeling of products. An intended use on the label has not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Iris Scissors Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Tip protector may fall off within the packaging, resulting in compromised...

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

Class II — Potential Health HazardOngoing
FoodOctober 18, 2024· Fresh Express Incorpated

Recalled Item: Fresh Express Gourmet Cafe Chicken Caesar 5.75oz Recalled by Fresh Express...

The Issue: Potential Listeria Monocytogenes Contamination. The pre-packaged condiment...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 18, 2024· Fresh Express Incorpated

Recalled Item: Fresh Express Gourmet Cafe Santa Fe Greek 5.2 oz Recalled by Fresh Express...

The Issue: Potential Listeria Monocytogenes Contamination. The pre-packaged condiment...

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

Class I — Serious Health HazardOngoing
Refund