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. 2,499 recalls have been distributed to Oregon in the last 12 months.
Showing 21921–21940 of 28,488 recalls
Recalled Item: Alaris Syringe Pump Recalled by CareFusion 303, Inc. Due to Channel Error...
The Issue: Channel Error code is displayed on the PC unit with an audio and visual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and...
The Issue: The cutting efficiency of the Countersinks was out of specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concave Reamer Head Recalled by Trilliant Surgical Ltd. Due to The...
The Issue: The cannulation of the Concave and Convex Reamer Heads may be too small to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tiger Cannulated Tray Lid Part # 210-00-001-1 NON-STERILE Recalled by...
The Issue: Sterilization tray lids for the Tiger and Tiger Headless Cannulated Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.0/4.0 Cannulated Drill Bit Recalled by Trilliant Surgical Ltd. Due to The...
The Issue: The cannulation of the 3.0/4.0 Cannulated Drill Bit inner diamter is too...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Spine Endoskeleton Locking Bone Screw Assembly Recalled by TITAN...
The Issue: Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune 2 Waste Management System Docking Station (120V and 230V) Recalled...
The Issue: The Fluid Coupling Sleeve, a component within the Neptune Waste Management...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Passive Biopsy Needle Kit Recalled by Medtronic Navigation, Inc....
The Issue: The adhesive between the sphere assembly and the biopsy needle shaft may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PET Discovery ST 16 Recalled by GE Healthcare Due to Potential for expulsion...
The Issue: Potential for expulsion of the Power Supply on Lightspeed CT scanner or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Passive Biopsy Needle Kit Recalled by Medtronic Navigation, Inc....
The Issue: The adhesive between the sphere assembly and the biopsy needle shaft may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wall Chart for STERRAD 100NX System Recalled by Advanced Sterilization...
The Issue: Advanced Sterilization PRoducts (ASP) is recalling the Wall Chart for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lightspeed 16 CT Recalled by GE Healthcare Due to Potential for expulsion of...
The Issue: Potential for expulsion of the Power Supply on Lightspeed CT scanner or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PET Discovery LS Recalled by GE Healthcare Due to Potential for expulsion of...
The Issue: Potential for expulsion of the Power Supply on Lightspeed CT scanner or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO Disk Recalled by Microbiologics Inc Due to LYFO Disk Catalog #0983L is...
The Issue: LYFO Disk Catalog #0983L is to contain Candida tropicalis. However, lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Naturalyte Liquid Bicarbonate Concentrate 6.4 liter bottle A Dialysate...
The Issue: Expansion of recall to lots manufactured in 2015 due to the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 Ventilator System Recalled by Covidien LP (formerly...
The Issue: Reports in which tidal volumes reaching patients were lower than set tidal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ottobock Pheon 3R62 Knee Joint The 3R62 Pheon is a Recalled by Otto Bock...
The Issue: Otto Bock Healthcare GmbH is voluntarily recalling all 3R62 Pheon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Robotic Arm Interactive Orthopedic (RIO) system component PN#205143 (locking...
The Issue: The locking pin on the RIO Base Array is damaged during assembly onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EnVeo R Loading System Recalled by Medtronic Cardiovascular Surgery-the...
The Issue: Medtronic is recalling the EnVeo R Loading Systems because of the presence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iChemVELOCITY Automated Urine Chemistry Catalog No. 800-3049 Recalled by...
The Issue: Iris International is recalling the iChemVELOCITY systems because they do...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.