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. 2,457 recalls have been distributed to Oregon in the last 12 months.
Showing 28321–28340 of 50,914 recalls
Recalled Item: 2008T Recalled by Fresenius Medical Care Renal Therapies Group, LLC Due to...
The Issue: While reviewing documentation for the next software release of the 2008T, an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Network Firewall (Cisco ASA 5506) Recalled by Philips Electronics...
The Issue: Firewall installed with Philips IntelliVue Information Center iX or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK(R) from TELEFLEX Auto Endo5(R) Recalled by Teleflex Medical Due to The...
The Issue: The product has a non-conformity that may cause clips to mislead, jam or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betadine Solution Swabstick Povidone-Iodine Solution USP Recalled by Purdue...
The Issue: Subpotent Drug: The laminate used to make the pouches was reversed such that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Famotidine tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Famotodine has an out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Difco" Agar Noble Recalled by Becton Dickinson & Co. Due to Mislabeling
The Issue: HighPuragar was mislabeled and inadvertently sold as Noble Agar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sirus Drill 13mm diameter trauma instrument used for preparation of Recalled...
The Issue: The Sirus Drill and Flexible Shaft instruments may not be adequately cleaned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Shaft hip and anatomical shoulder instrument used for preparation...
The Issue: The Sirus Drill and Flexible Shaft instruments may not be adequately cleaned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Go.Up computed tomography (CT) x-ray system table Recalled by...
The Issue: The table may become unstable if the nuts on the bolts were not adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS CL Flow Cytometer Recalled by Beckman Coulter Inc. Due to The system...
The Issue: The system may duplicate sample requests leading to sample misidentification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemosphere System with the following three components: HEM1 Advanced Monitor...
The Issue: Pre-procedural issues related to software defects
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Go.Now computed tomography (CT) x-ray system table Recalled by...
The Issue: The table may become unstable if the nuts on the bolts were not adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bisoprolol Fumarate tablets Recalled by Unichem Pharmaceuticals Usa Inc Due...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification for an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: O-arm¿ O2 interventional fluoroscopic x-ray system Recalled by Medtronic...
The Issue: During servicing of certain internal components of the O-Arm O2 Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Knee...
The Issue: Knee implant components (tibial bearings) are labeled with the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Knee...
The Issue: Knee implant components (tibial bearings) are labeled with the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Costco item # 1052939 Recalled by Tai Foong USA Inc Due to Undeclared Egg
The Issue: Royal Asia brand Shrimp Wonton Noodle Soup is recalled due to undeclared egg.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Birds Eye Baby Sweet Peas Recalled by Pinnacle Food Group, Llc Due to...
The Issue: Product has the potential to be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Artis zee and Artis zeego model Interventional fluoroscopic x-ray foot...
The Issue: The possibility exists for the wireless foot switch to fail due to impacts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-900 Automated Immunoassay Analyzer performs three methods of...
The Issue: The firm has become aware of a potential issue that may affect the mixing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.