Product Recalls in Hawaii
Product recalls affecting Hawaii — including food, drugs, consumer products, medical devices, and vehicles distributed to Hawaii. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,519 recalls have been distributed to Hawaii in the last 12 months.
Showing 11481–11500 of 27,645 recalls
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: 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.
Recalled Item: VITROS XT 7600 Integrated System Software Versions 3.5.1 and below Recalled...
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 below Product...
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 3600 Immunodiagnostic System - Product Code: 6802914 Unique Recalled...
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: Philips SureSigns VM1SpO2 Recalled by Philips North America, LLC Due to...
The Issue: Philips has identified a Philips SureSigns VM1 monitor in the possession of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.