Product Recalls in Washington
Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,766 recalls have been distributed to Washington in the last 12 months.
Showing 11801–11820 of 29,208 recalls
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 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 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: 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: 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: 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 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: Leica ARveo and M530 OH6 microscope systems. Recalled by Leica Microsystems,...
The Issue: Possible unintended interruption of surgical procedures due to equipment...
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: 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 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 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: 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.
Recalled Item: RayStation 8B Service Pack 2 Recalled by RAYSEARCH LABORATORIES AB Due to...
The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.