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. 2,677 recalls have been distributed to Kentucky in the last 12 months.
Showing 61–80 of 28,748 recalls
Recalled Item: Atellica CH Urine Albumin (UAlb). Material Number: 11537225 Recalled by...
The Issue: Falsely depressed UAlb patient results may occur. Affected samples with any...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas pro integrated solutions with cobas c 503 analytical units: Recalled...
The Issue: Software defect, which allows the system to accept erroneous, non-monotonous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...
The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM Premier 5000 PAK Recalled by Instrumentation Laboratory Due to Confirmed...
The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM Premier 5000 PAK Recalled by Instrumentation Laboratory Due to Confirmed...
The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: (1)...
The Issue: Potential packaging failures, which could lead to a breach in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Private Label CVS. Model Number: CVS405406. Helps maintain a moist Recalled...
The Issue: Potential packaging failures, which could lead to a breach in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus High Flow Insufflation Unit. Model Number: UHI. Used for Recalled by...
The Issue: Issue with software algorithm which may lead to overpressure events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Centricity Universal Viewer Zero Footprint Client Recalled by...
The Issue: Under certain workflows, patient information shown in the viewer may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus High Flow Insufflation Unit. Model/ Number: UHI-2. Used for Recalled...
The Issue: Issue with software algorithm which may lead to overpressure events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDIHONEY CALCIUM ALGINATE WITH ACTIVE LEPTOSPERMUM HONEY. Model Numbers:...
The Issue: Potential packaging failures, which could lead to a breach in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus High Flow Insufflation Unit. Model Number: UHI-3. Used for Recalled...
The Issue: Issue with software algorithm which may lead to overpressure events.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP HUMERAL...
The Issue: Knee and Humeral socket implants contain incorrect labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS Recalled by...
The Issue: Knee and Humeral socket implants contain incorrect labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING Recalled by...
The Issue: There is the potential for the length of the trocar shaft to be too long.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP STANDARD...
The Issue: Knee and Humeral socket implants contain incorrect labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIE PAK Models: P2HC-A Recalled by Edermy LLC Due to Lack of 510K clearance
The Issue: Lack of 510K clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIE Trolley System Model: 2005 Recalled by Edermy LLC Due to Lack of 510K...
The Issue: Lack of 510K clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laerdal Compact Suction Unit 4 RTCA version (LCSU 4 RTCA) 1) LCSU 4 Recalled...
The Issue: units manufactured in a limited time period may emit electromagnetic noise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Octopus Nuvo Tissue Stabilizer Recalled by Medtronic Perfusion Systems Due...
The Issue: During the manufacturing, Medtronic personnel identified an assembly issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.