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. 2,447 recalls have been distributed to Oregon in the last 12 months.
Showing 35121–35140 of 50,914 recalls
Recalled Item: Ellipse ICD (Implantable Cardioverter Defibrillator) Model CD2411-36Q...
The Issue: St. Jude Medical is recalling the Ellipse ICD (Implantable Cardioverter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CF InPlex ASR Card Recalled by Hologic, Inc Due to Complaints of false...
The Issue: Complaints of false positive HET mutations and leaking cards; could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hologic InPlex CF Molecular Test (IVD) Recalled by Hologic, Inc Due to...
The Issue: Complaints of false positive HET mutations and leaking cards; could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Ray Diagnostic Table Recalled by Shimadzu Medical Systems Due to Report of...
The Issue: Report of unintentional movement of table to reverse tilting.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mach 4 Mouse Probe vial within the Mach 4 Universal HRP-Polymer Kit Recalled...
The Issue: Biocare Medical has identified a single lot (082715) of its Mach 4 HRP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Ultracot 15 mm x 15 mm (Glassine) by American Surgical...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Ray-Cot 1/2" x 3" : 60-09 Product Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Policot 1/2" x 1/2" : 90-06 Product Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LGD-Xtreme (ligandrol LGD-4033) Recalled by Invisiblu International LLC Due...
The Issue: Marketed Without An Approved NDA/ANDA: Contains an unapproved drug,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibrate Capsules (Micronized) Recalled by Amerisource Health Services...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibrate Capsules (Micronized) Recalled by Amerisource Health Services...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: E.cam or Symbia systems that use foresight detectors - Product Recalled by...
The Issue: E. CAM and Symbia system with foresight detectors performing gated or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ondansetron Tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications; 12 month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADVIA Centaur CP Immunoassay System Recalled by Siemens Healthcare...
The Issue: The firm identified an issue in sample processing when using EZee-Nest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pleur-evac Chest Drainage System Recalled by Teleflex Medical Due to The...
The Issue: The label on the Tyvek bag is missing. This is used by customers to identify...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Yogurt Super Soynuts packaged in 16 oz. plastic bags and Recalled by Lee...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Merge PACS software. Product Usage: Merge PACS (Picture Archiving...
The Issue: The software did not show unviewed images when the last view was skipped....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PneumoSure XL High Flow Insufflator and PneumoSure High Flow Insufflator...
The Issue: When operating the device in high flow mode (40L/min, 15 mmHg) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ DIAGNOSTIC ULTRASOUND SYSTEM Recalled by Philips Ultrasound, Inc. Due...
The Issue: The fasteners securing the control panel assembly to the base of the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific is voluntarily implementing a Medical Device Recall of one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.