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. 2,672 recalls have been distributed to Kentucky in the last 12 months.
Showing 2701–2720 of 28,748 recalls
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: human med Biofill Infiltration Cannula Recalled by HUMAN MED AG Due to The...
The Issue: The cannula tubes do not comply with the specification. The water jet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Essenz HLM (Heart-Lung Machine) Recalled by LivaNova Deutschland GmbH Due to...
The Issue: Heart-Lung Machine GUI touchscreen may go dark for 10-15 seconds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CorNeat EverPatch Recalled by CORNEAT VISION, LTD. Due to Retroactive; Due...
The Issue: Retroactive; Due to complaints, labeling correction for permanent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) COMBINED SPINAL AND EPIDURAL...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smaxel Fractional CO2 Laser Recalled by IDS LTD Due to The Smaxel Fractional...
The Issue: The Smaxel Fractional CO2 Laser does not include a Certification label, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.