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. 2,601 recalls have been distributed to Kentucky in the last 12 months.
Showing 13361–13380 of 28,748 recalls
Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...
The Issue: Acetabular liners failed the oxidation testing performed prior to release....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...
The Issue: Acetabular liners failed the oxidation testing performed prior to release....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...
The Issue: Acetabular liners failed the oxidation testing performed prior to release....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Folate 100 test kit-for IVD of folate Recalled by...
The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Folate (500 Test Kit)-for IVD of folate Recalled by...
The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Folate (500 Test Kit )- for IVD Recalled by Siemens...
The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynex DSX Software-IVD ELISA Assays effected as follows: DSX Assay Recalled...
The Issue: Assay files used on the open Dynex DSX Instrument to process IVD ELISA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge MCC Flow i Disposable CO2 absorber Recalled by GETINGE US SALES LLC...
The Issue: Reversed expiration and manufacturing date on the label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Enteral Safe Feeding Tubes: a) Recalled by DeRoyal Industries Inc...
The Issue: Certain MED-RX Polyurethane Feeding Tubes are being recalled due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NobelActive Internal NP 3.5x15mm Endosseus dental implant Recalled by Nobel...
The Issue: The top label for dental implant may incorrectly indicate the implant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Complaints have been received...
The Issue: Complaints have been received regarding difficulty in removing the driver...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Complaints have been received...
The Issue: Complaints have been received regarding difficulty in removing the driver...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips 5-Lead Set Recalled by Philips North America, LLC Due to The...
The Issue: The thickness of the connector to the trunk cable on affected limb lead sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm FDR Go Plus mobile X-ray system Recalled by Fujifilm Medical...
The Issue: The graphics driver of the FDR Go PLUS might cause the appearance of a Blue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-TEMP LT System Recalled by Cincinnati Sub-Zero Products LLC, a...
The Issue: Updated Manual-Warnigs have been added stating that exceeding 40'C for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman ISOCOOL Bipolar Forceps-are indicated for cauterizing Recalled by...
The Issue: Tips have an inadequate product insulation coating, which could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit-catheter permits venous access to central...
The Issue: Arrow AGB+ Multi-Lumen CVC Kit - lidstock incorrectly states within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas e 601 module (cobas 6000 Modular Series system) Part Number:...
The Issue: Quality issue with high pressure solenoid valves may cause inaccurate results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas c513 Analyzer Recalled by Roche Diagnostics Operations, Inc. Due to...
The Issue: Quality issue with high pressure solenoid valves
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas 8000 Modular Analyzer Series: cobas 8000 ISE module part Recalled by...
The Issue: Quality issue with high pressure solenoid valves
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.