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. 2,470 recalls have been distributed to Oregon in the last 12 months.
Showing 24901–24920 of 28,488 recalls
Recalled Item: Model Kodak 2100 Intraoral X-Ray System Recalled by Carestream Health Inc....
The Issue: Carestream received problem reports relating to apparent early failure of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Model: 861290 The HeartStart...
The Issue: HeartStart XL+ battery charge time to 100% capacity at 35¿C (95¿F) is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaSure Impedance Controlled Endometrial Ablation System Radiofrequency...
The Issue: NovaSure Radiofrequency Control Units may not meet a requirement of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeCare 5000 Pump (Plum 1.6) infusion pump Recalled by Hospira Inc. Due to...
The Issue: There is the potential for the door roller assembly on the Plum LifeCare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum XL Recalled by Hospira Inc. Due to There is the potential for the door...
The Issue: There is the potential for the door roller assembly on the Plum LifeCare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable Clip Applier Manufactured by AtriCure Recalled by Atricure Inc Due...
The Issue: The firm was notified by a customer of a cracked spring in the handle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartSite Needleless Connector Recalled by CareFusion 303, Inc. Due to...
The Issue: CareFusion is recalling the SmartSite Needlefree Connector, model number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buzzaround XL scooters' Product Usage: mobility Recalled by Golden...
The Issue: Buzzaround XL scooters' front to rear lockup can become unintentionally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: HER2 CISH pharmDx Kit Catalog/Model number: SK109 Recalled by...
The Issue: Dako has initiated a recall of HER2 CISH pharmDxTM Kit because weak red...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D and Proteus XR/a equipped with Wireless...
The Issue: GE Healthcare has recently become aware of a software issue associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA Multical. ABX PENTRA N Control. ABX PENTRA P Recalled by Horiba...
The Issue: HORIBA Medical is informing all ABX PENTRA MultiCal, N Control, and P...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crimper Model 9100CR26 The Crimper is indicated for use in Recalled by...
The Issue: Edwards Lifesciences is recalling two lot numbers of the 26mm transcatheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDITECH Microbiology - Calculator/data processing module Recalled by...
The Issue: Potential for patient results being removed from LAB/EMR.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trifurcated Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion...
The Issue: CareFusion is recalling the Trifurcated Extension Set, models ME 1224 and MP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal ST. Circumcision Clamp Recalled by DeRoyal Industries Inc Due to...
The Issue: Three lots of circumcision clamps were manufactured out of specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products 25-OH Vitamin D Total Calibrators Recalled...
The Issue: Ortho Clinical Diagnostics has determined that the VITROS Immunodiagnostic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The FOCUS is a microprocessor controlled intra-oral x-ray unit with Recalled...
The Issue: Instrumentarium Dental has delivered a number of FOCUS 3.0 Intraoral X-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accuray CyberKnife Robotic Radiosurgery System Recalled by Accuray...
The Issue: Potential Safety issue with Synchrony Boom Arm Mounting Assembly - one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InnerCool RTx Endovascular System Recalled by Philips Healthcare Due to...
The Issue: Phillips Healthcare initiated this action because the Main Control Board...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Flu A/B & RSV Direct assay Recalled by Focus Diagnostics Inc Due to...
The Issue: Focus Diagnostics is initiating an urgent safety notice correction for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.