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. 2,616 recalls have been distributed to Oregon in the last 12 months.
Showing 10821–10840 of 28,488 recalls
Recalled Item: Evolut (TM) R System. With the following model numbers: a. EVOLUTR-23...
The Issue: Potential for Transcatheter Aortic Valve (TAV) leaflet damage when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Biomeme SARS-CoV-2 Real-Time RT-PCR Test is a molecular in Recalled by...
The Issue: The firm has become aware of nine reports by a single customer that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Box Label: ION Fully Articulating Catheter Recalled by Intuitive Surgical,...
The Issue: The distal tip ring of the fully articulating catheter may become dislodged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viral Transport Medium Recalled by Hardy Diagnostics Due to There is a...
The Issue: There is a potential for contamination within Viral Transport Media. Use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolut (TM) PRO System. With the following model numbers: a. EVOLUTPRO-23...
The Issue: Potential for Transcatheter Aortic Valve (TAV) leaflet damage when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolut (TM) PRO+ System. With the following model numbers: a. Recalled by...
The Issue: Potential for Transcatheter Aortic Valve (TAV) leaflet damage when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee floor Recalled by Siemens Medical Solutions USA, Inc Due to Some...
The Issue: Some electronic components within the generator were equipped with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViewRay MRIdian System: Model No. 10000 Recalled by Viewray, Inc. Due to...
The Issue: There is a potential that components of the receive coil can reach elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViewRay MRIdian Linac System: Model No. 20000 Recalled by Viewray, Inc. Due...
The Issue: There is a potential that components of the receive coil can reach elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Geistlich Bio-Oss Pen 0.25-1mm 0.5g - Product Usage: natural bone Recalled...
The Issue: Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Geistlich Bio-Oss Pen 0.25-1mm 0.25g - Product Usage: natural bone Recalled...
The Issue: Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Geistlich Bio-Oss Pen 1-2mm 0.5g - Product Usage: natural bone Recalled by...
The Issue: Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250i Recalled by Mevion Medical Systems, Inc. Due to Treatment beam...
The Issue: Treatment beam information disappears on Treatment Console screen while beam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 (PB980) Ventilator Series - Product Usage: for Recalled...
The Issue: In-house lab observations and customer reports of overheating and/or thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Zyphr Disposable Cranial Perforator Recalled by Stryker Instruments...
The Issue: Potential for the inner bit to contain a crack, that may or may not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.