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. 2,637 recalls have been distributed to Oregon in the last 12 months.
Showing 9301–9320 of 28,488 recalls
Recalled Item: MERITMEDICAL Prelude Short Sheath Introducer Recalled by Merit Medical...
The Issue: There is a potential that a package sheath contains an incorrect dilator.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CritiCool Recalled by Belmont Instrument Corporation Due to Premature pump...
The Issue: Premature pump failure may lead to the device displaying a HALT 4 error,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Braun ThermoScan PRO 6000 Ear Thermometer-indicated for the intermittent...
The Issue: If the device is exposed to fluid ingress and is used before the cleaning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solero Generator US PG Recalled by Angiodynamics, Inc. Due to Specific...
The Issue: Specific serial numbers of the Solero MTA Generator require servicing to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nihon Kohden NKV-550 Ventilator Recalled by NIHON KOHDEN ORANGEMED, INC Due...
The Issue: Potential defective gas inlet pressure regulator within ventilator which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solero Generator US PG Recalled by Angiodynamics, Inc. Due to Specific...
The Issue: Specific serial numbers of the Solero MTA Generator require servicing to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solero Generator PG Recalled by Angiodynamics, Inc. Due to Specific serial...
The Issue: Specific serial numbers of the Solero MTA Generator require servicing to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solero Generator PG Recalled by Angiodynamics, Inc. Due to Specific serial...
The Issue: Specific serial numbers of the Solero MTA Generator require servicing to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONICHD 1000i Shears (36cm Shaft Length)-indicated for soft tissue...
The Issue: An internal component may be cracked and become lodged behind the energy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC HD 1000i Shears (20cm Shaft Length)-indicated for soft tissue...
The Issue: An internal component may be cracked and become lodged behind the energy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Blood Culture Identification (BCID) Panel Product Pouch Label:...
The Issue: Due to product complaints received for false negative results (dropouts)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis SABER PTA Balloon Dilation Catheter Recalled by Cordis Corporation...
The Issue: The balloon protective sheath may potentially be contaminated with a foreign...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Recalled by Philips North America LLC Due to Infant/Child...
The Issue: Infant/Child defibrillator pads contain incorrect labeling. This could lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by Teleflex...
The Issue: The firm received reports that the endotracheal tube cuff could be inflated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Endotracheal Tube oral/nasal Murphy Eye Recalled by Teleflex Medical...
The Issue: The firm received reports that the endotracheal tube cuff could be inflated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Endotracheal Tube oral/nasal Magill Recalled by Teleflex Medical...
The Issue: The firm received reports that the endotracheal tube cuff could be inflated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Flexi-Set Cuffed Endotracheal Tube and Stylet Set Recalled by Teleflex...
The Issue: The firm received reports that the endotracheal tube cuff could be inflated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Normand Remisol Advance Data Manager Recalled by Beckman Coulter Inc. Due to...
The Issue: There is a potential that the data management system may add additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Antibodies Recalled by Cell Marque Corporation Due to Mouse...
The Issue: Mouse Monoclonal Antibody labelled with an incorrect expiry date of 31 Dec...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gastroscope Family # 1-Gastroscopes without a Water Jet Channel Models:...
The Issue: Updated Reprocessing Instruction For Use (rIFU): Impacted PENTAX Medical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.