Product Recalls in Oregon
Product recalls affecting Oregon — including food, drugs, consumer products, medical devices, and vehicles distributed to Oregon. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,557 recalls have been distributed to Oregon in the last 12 months.
Showing 18721–18740 of 50,914 recalls
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: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Some bottles may contain mixed strengths of the product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NP Thyroid 30 Recalled by Acella Pharmaceuticals, LLC Due to Superpotent Drug.
The Issue: Superpotent Drug.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doxycycline Hyclate Tablets Recalled by The Harvard Drug Group Due to Failed...
The Issue: Failed Dissolution Specification: The dissolution test at the 24 month time...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NP Thyroid 90 Recalled by Acella Pharmaceuticals, LLC Due to Superpotent Drug.
The Issue: Superpotent Drug.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Some bottles may contain mixed strengths of the product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NP Thyroid 60 Recalled by Acella Pharmaceuticals, LLC Due to Superpotent Drug.
The Issue: Superpotent Drug.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Some bottles may contain mixed strengths of the product.
Recommended Action: Stop taking this medication. Contact your pharmacy or 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.
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: 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: Zilretta (triamcinolone acetonide extended-release injectable suspension)...
The Issue: Temperature Abuse: Product was stored at room temperature longer than 6...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.