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. 2,641 recalls have been distributed to Oregon in the last 12 months.
Showing 8461–8480 of 28,488 recalls
Recalled Item: Atellica CH Lithium_2 (LITH_2) Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Enzymatic Hemoglobin A1c (A1c_E/A1c_H) Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Calcium_2 (CA_2) Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 SYPH T PACK Syphilis Total & RPR Reagent Pack Recalled by...
The Issue: Due to current concerns related to COVID-19 vaccine interference with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 Syphilis Total & RPR Calibrator Set CAL Recalled by Bio-Rad...
The Issue: Due to current concerns related to COVID-19 vaccine interference with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The IFU for the Autoclavable Temperature Probes: Part # 453564635891...
The Issue: Update to instructions for use regarding the cleaning and disinfection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brius Patient Specific Brackets (components in a set of custom Recalled by...
The Issue: Pontics, brackets, and customized orthodontic appliances were sold and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Customized Brius Appliances (custom metal orthodontic devices) Recalled by...
The Issue: Pontics, brackets, and customized orthodontic appliances were sold and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brius Pontics (components in a set of custom metal orthodontic devices)...
The Issue: Pontics, brackets, and customized orthodontic appliances were sold and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Recalled by Philips North America LLC Due to There is a potential...
The Issue: There is a potential for AED pads to experience gel separation from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Recalled by Philips North America LLC Due to There is a potential...
The Issue: There is a potential for AED pads to experience gel separation from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic TurboHawk Plus Directional Atherectomy System 6F Recalled by ev3...
The Issue: The device has similarities in design to another device that the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic TurboHawk Plus Directional Atherectomy System 6F Recalled by ev3...
The Issue: The device has similarities in design to another device that the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiovascular Procedure Kit catalog # 76645 & 73806 Recalled by Terumo...
The Issue: Potential for Cardiovascular Procedure Kit packaging damage that occurred...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MM-TSM (Touch Screen Module/Secondary Controller/Bedside Controller)...
The Issue: Multi-Modality Touch Screen Modules (MM-TSM), used with integrated IVUS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity s System software version2.8.0 Recalled by Abbott Laboratories, Inc...
The Issue: Software error associated with the immunoassay analyzer wash cycle which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips StentBoost Live R2.0 application Recalled by Philips Healthcare Due...
The Issue: Due to an incorrect configuration setting in the EPX database of StentBoost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura (Model Numbers 722010 Recalled by Philips North America Llc...
The Issue: Due to a software defect, the Philips StentBoost Live R2.0 might not process...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NuOss Collagen Block Size 8mm x 9mm x 9mm- used Recalled by Ace Surgical...
The Issue: NuOss Collagen (dental) was packaged with a Collatene Fibrillar Collagen(for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) JOBST Compri2 Recalled by BSN Medical Inc Due to Mislabeling
The Issue: The folding boxes within the shipping case are mislabeled. The shipping case...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.