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. 2,602 recalls have been distributed to Kentucky in the last 12 months.
Showing 11701–11720 of 28,748 recalls
Recalled Item: Thora-Para 8 Fr Catheter Drainage Tray w/o Lidocaine Recalled by Carefusion...
The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safe-T-Centesis 6 Fr Catheter Drainage Tray Recalled by Carefusion 2200 Inc...
The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thora-Para 8 Fr Catheter Drainage Tray Recalled by Carefusion 2200 Inc Due...
The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safe-T 5 Fr Thora-Para Tray With 5 Fr. Catheter and Recalled by Carefusion...
The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safe-T 8 Fr Thora-Para Tray With 8 Fr. Catheter and Recalled by Carefusion...
The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thora-Para 5 Fr Non-Valved Catheter Drainage Tray Recalled by Carefusion...
The Issue: The Universal Drainage Set (UDS) may contain valves that leak internally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH...
The Issue: Lack of assurance of sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prodimed Combicath Paediatric catheters for blind protected distal bronchial...
The Issue: Lack of assurance of sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH...
The Issue: Lack of assurance of sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prodimed Combicath catheters for blind or fibrescope-guided protected distal...
The Issue: Lack of assurance of sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prodimed Combicath Paediatric catheters for blind protected distal bronchial...
The Issue: Lack of assurance of sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prodimed Combicath catheters for blind or fibrescope-guided protected distal...
The Issue: Lack of assurance of sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood gases (PCO2 Recalled by Radiometer Medical ApS Due to Potential risk...
The Issue: Potential risk of patient mix-up on analyzers due to software issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood gases (PCO2 Recalled by Radiometer Medical ApS Due to Potential risk...
The Issue: Potential risk of patient mix-up on analyzers due to software issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON AcuNav Volume Intracardiac Echocardiography Catheter 12.5F Recalled...
The Issue: Due to adverse events received by the firm for left atrial perforations and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm Synapse PACS Software Version 5.5.x and 5.7.x- intended as Recalled...
The Issue: Lateromedial (LM) and Lateromedial Oblique (LMO) Orientation Markers may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-900 Analyzer Recalled by Tosoh Bioscience Inc Due to The Substrate...
The Issue: The Substrate Monitoring System in the AIA-900 Analyzer did not detect an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VistaSolution Recalled by Vitalconnect Inc. Due to A healthcare provider...
The Issue: A healthcare provider (HCP) noticed a patient had a lowered historic SpO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System Software Versions 3.3.3 and below...
The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System - Software Versions 3.3.3 and Recalled by...
The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.