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. 2,641 recalls have been distributed to Oregon in the last 12 months.
Showing 8441–8460 of 28,488 recalls
Recalled Item: Cook Celect PlatinumVena Cava Filter Set Catalog Number/GPN:...
The Issue: IFU update includes an update to the Device description, Intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Babylog VN500 Ventilator with Software 2.51.01 and Lower- intended for...
The Issue: Cybersecurity Improvement Action-not equipped against potential cyber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cytocell 8 Square Template Slides (Glass)- microscope slides : PCN008...
The Issue: Labelled with an incorrect expiry date on the outer label with an extended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compella Therapy Air Supply Unit Recalled by Baxter Healthcare Corporation...
The Issue: Potential damage to the power cord may cause the power conductors to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET TRAUMA A.L.P.S. FIBULA COMPOSITE LOCKING PLATE 8 HOLE Recalled by...
The Issue: Packaging of various implants may not have sufficient adhesion on all sides,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET Sports Medicine JUGGERLOC SLOTTED REAMER: [Item # 110010371 Recalled...
The Issue: Packaging of various implants may not have sufficient adhesion on all sides,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET TRAUMA Drill Bit Recalled by Biomet, Inc. Due to Packaging of various...
The Issue: Packaging of various implants may not have sufficient adhesion on all sides,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET Trauma Recalled by Biomet, Inc. Due to Packaging of various implants...
The Issue: Packaging of various implants may not have sufficient adhesion on all sides,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compella Bariatric Bed System Recalled by Baxter Healthcare Corporation Due...
The Issue: Potential damage to the power cord may cause the power conductors to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 1.1 (709031) Recalled by PHILIPS MEDICAL SYSTEMS Due to...
The Issue: While performing a fluoroscopy examination, there is a potential that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 1.0 (709030) Recalled by PHILIPS MEDICAL SYSTEMS Due to...
The Issue: While performing a fluoroscopy examination, there is a potential that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUNTLEIGH Disposable intraoperative Probe Recalled by Huntleigh Healthcare...
The Issue: Faceplate may become detached from the probe body.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4-11B Recalled by RaySearch America Inc Due to Incorrect source...
The Issue: Incorrect source to skin or surface distance (SSD) calculation may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m Integrated Reaction Units (IRU) Recalled by Abbott Molecular, Inc....
The Issue: There is potential for the Reaction Vessels (RVs) detaching from the RV cap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 3.5 Middle and 3.2 Proximal Saw Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System Driver SKU: NX-DR Orthopedic surgical...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 3.5 Middle 3.2 Proximal Kit SKU: Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 4.5 Middle 3.2 Proximal Kit SKU: Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Hammertoe Correction System 4.5 Middle and 3.2 Proximal Saw Recalled...
The Issue: Proximal end of the driver is oversized in varying degrees, making it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Fructosamine (Fruc) Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.