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. 2,609 recalls have been distributed to Oregon in the last 12 months.
Showing 11701–11720 of 50,914 recalls
Recalled Item: Surpria 64: Software Version V3.11 Recalled by FUJIFILM Healthcare Americas...
The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCENARIA View: Software Version V1.08 Recalled by FUJIFILM Healthcare...
The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surpria: Software Version V3.11 Recalled by FUJIFILM Healthcare Americas...
The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Sensis or Sensis Vibe Combo systems as follows: System Recalled by...
The Issue: The Sensis Signal Input Box provides hooks as a milled item on the bottom of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...
The Issue: Distributed VTM outside of VTM Guidance and without clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...
The Issue: Distributed VTM outside of VTM Guidance and without clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...
The Issue: Distributed VTM outside of VTM Guidance and without clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tacrolimus Ointment Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: Defective Container: Tube split from side seam
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ativan Injection (lorazepam injection Recalled by Hikma Pharmaceuticals USA...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SafeControl handset (a component of the Sentida bed which moves Recalled by...
The Issue: When the handset is disconnected from the power mains, and mains operation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERA 3000 Hepatic Artery Infusion Pump Recalled by Intera Oncology, Inc....
The Issue: Higher than expected flow rate.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aripiprazole Tablets Recalled by Apotex Corp. Due to Failed dissolution...
The Issue: Failed dissolution specifications: OOS for dissolution at the 12-month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lemon Muffins Recalled by Portland Specialty Baking LLC Due to Plastic material.
The Issue: Plastic material.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: T-Cell Xtend .610 US Recalled by OXFORD IMMUNOTEC LTD Due to Due to...
The Issue: Due to equipment failure, affected products were stored at temperatures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T-SPOT.TB .300 US Recalled by OXFORD IMMUNOTEC LTD Due to Due to equipment...
The Issue: Due to equipment failure, affected products were stored at temperatures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIM-V Medium .200/500 Recalled by OXFORD IMMUNOTEC LTD Due to Due to...
The Issue: Due to equipment failure, affected products were stored at temperatures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ShockPulse-SE Lithotripsy Generator Model/Serial: SPL-S Recalled by Olympus...
The Issue: Mis-wired component-the improperly wired component can result in additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.