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. 2,544 recalls have been distributed to Oregon in the last 12 months.
Showing 19421–19440 of 50,914 recalls
Recalled Item: AB HiResolution Bionic Ear System Recalled by Advanced Bionics, LLC Due to...
The Issue: hearing performance degradation due to body-fluid entering the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB HiResolution Bionic Ear System Recalled by Advanced Bionics, LLC Due to...
The Issue: hearing performance degradation due to body-fluid entering the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sticky Fingers Bakeries Gluten-Free Scones Recalled by Custom Foods LLC Due...
The Issue: Firm received customer inquiry of why wheat is listed in the ingredient list...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Cogent Hemodynamic Monitoring System. Recalled by ICU Medical, Inc. Due...
The Issue: Firm identified software issues which leads to the patient ID and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ev3 Pipeline Flex Embolization Device. For neurological endovascular use....
The Issue: Embolization device delivery system may fracture at the distal section...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Ethyl Alcohol Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The assay may exhibit a positive bias in QC and patient results within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS....
The Issue: Embolization device delivery system may fracture at the distal section...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q.zen Biplane Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A software issue could potentially cause the stand and table movements to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q Biplane Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A software issue could potentially cause the stand and table movements to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee Biplane Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A software issue could potentially cause the stand and table movements to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DFINE Vertebral Assemblies: Hydraulic-Master Syringe Assembly Recalled by...
The Issue: Vertebral hydraulic assemblies has incorrect expiration date printed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DFINE Vertebral Hydraulic Assemblies: Hydraulic Assembly Recalled by Merit...
The Issue: Vertebral hydraulic assemblies has incorrect expiration date printed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE MAGEC 2 Rod X.X mm XX mm Recalled by NuVasive Inc Due to...
The Issue: Post-implantation separation of an actuator end cap component that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnipod DASH Personal Diabetes Manager (PDM) Recalled by Insulet Corporation...
The Issue: In certain scenarios, the Omnipod DASH PDM may suggest an inaccurate bolus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Total Bilirubin_2 assay- SMN: 10341115 (40 mL) & Recalled by...
The Issue: Bilirubin assays may exhibit a positive bias with patients on eltrombopag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Total Bilirubin Flex reagent cartridge -In vitro Diagnostic for...
The Issue: Bilirubin assays may exhibit a positive bias with patients on eltrombopag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Total Bilirubin_2 assay-In vitro Diagnostic for the...
The Issue: Bilirubin assays may exhibit a positive bias with patients on eltrombopag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Direct Bilirubin_2 assay-SMN: 10316610 (20 mL) & 10341114...
The Issue: Bilirubin assays may exhibit a positive bias with patients on eltrombopag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Total Bilirubin Flex¿ reagent cartridge -In vitro...
The Issue: Bilirubin assays may exhibit a positive bias with patients on eltrombopag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Direct Bilirubin_2 assay In vitro Diagnostic for the Recalled by...
The Issue: Bilirubin assays may exhibit a positive bias with patients on eltrombopag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.