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. 2,567 recalls have been distributed to Oregon in the last 12 months.
Showing 15841–15860 of 28,488 recalls
Recalled Item: Temperature sensing catheter 14FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature sensing catheter 16FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensor Catheter 16FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensor Catheter 14FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Temperature Sensor Catheter 14FR Recalled by Degania Silicone, Ltd....
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percepta CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm and...
The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermistor Foley catheter Recalled by Degania Silicone, Ltd. Due to The...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Espiner Tissue Retrieval System-Eco-Sac Trocar 12mm Vol: 1200 ml...
The Issue: Label was incorrect. The label states that the volume of the retrieval bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Maestro 4000 Cardiac Ablation System Recalled by Boston...
The Issue: Reports of unintended continuation of radiofrequency (RF) energy delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed...
The Issue: Through investigation, it was determined that H12LP Trocars in scope of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NICO Shepherd' s Hook - Greenberg Recalled by Nico Corp. Due to Mislabeling
The Issue: Mislabeled hook pouch included a transport/storage label rather than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: J-Plasma Precise 360 Recalled by Bovie Medical Corporation Due to There is a...
The Issue: There is a potential risk associated with the PEEK tip of the J-Plasma...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPAP Mask Cushion Recalled by Compass Health Brands (Corporate Office) Due...
The Issue: A May 2015 design change in the cushion seal replacement part and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Oasis MRI system Product Usage: Hitachi MR system is Recalled by...
The Issue: The stainless steel belt which runs the length of the table underneath the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Cleaning Brush Recalled by Medline Industries Inc Due to There is...
The Issue: There is potential risk of brush detachment during cleaning. If brush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VOLISTA StandOP Surgical Light Recalled by Maquet SAS Due to Certain VOLISTA...
The Issue: Certain VOLISTA StandOP Surgical Lights have been identified as having a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arctic Sun Temperature Management System Recalled by Bard Medical Division...
The Issue: An improper wiring connection on the chiller assembly may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Biosystems HistoCore SPECTRA ST Recalled by Leica Microsystems, Inc....
The Issue: These devices have an incorrect specification against safety standard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY BCS Knee Conventional Polyethylene Inserts: 74023111 Recalled by...
The Issue: The data in the National Joint Registry of England, Wales and Northern...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.