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. 2,457 recalls have been distributed to Oregon in the last 12 months.
Showing 27521–27540 of 28,488 recalls
Recalled Item: SPECIALTY AUDIBLE TORQUE WRENCH Recalled by Stryker Spine Due to Multiple...
The Issue: Multiple complaints have reported the hex tip of the torque wrench...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra HRAIM Head Ring Assembly with Intubation Mounts The CRW Recalled by...
The Issue: T-handle screw is used on a complementary product to the CRW, the Integra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra CRW Precision Arc (CRWPRECISE) Recalled by Integra LifeSciences...
The Issue: T-handle screw is used on a complementary product to the CRW, the Integra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista(R) Systems Vista(R) Theophylline THEO Flex(R) Regent...
The Issue: Firm has received complaints from customers of "Abnormal Reaction" errors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGFA IMPAC CV DICOMStore with Media Purge Daemon (MPD) and Recalled by AGFA...
The Issue: Loss of patient data can occur under certain circumstances due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmeriWater MRO Dialysis RO+ System Recalled by AmeriWater Inc Due to The...
The Issue: The firm was notified that a malfunction of the device was caused by an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker MANTIS TORQUE WRENCH Manufactured by: Stryker pine Recalled by...
The Issue: Multiple complaints have reported the hex tip of the torque wrench...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Positron Emission Tomography (PET) and X-ray Computed Tomography Recalled by...
The Issue: Philips became aware of an issue relating to a UPS battery cabinet that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Devices includes a Multi Port Inflator or without Multi Port Recalled by...
The Issue: Parks Medical Electronics, Inc. was made aware of two incidents where an air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 16 Fr HemoStar XK Long-Term Hemodialysis Catheter Recalled by Bard Access...
The Issue: Bard Access Systems is recalling one lot of 16 Fr HemoStar XK Long Term...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Prolactin Assay: ADVIA Centaur Calibrator B Catalog Number....
The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur FSH Assay: ADVIA Centaur Calibrator B US: Calibrator Recalled...
The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare conducted...
The Issue: GE Healthcare conducted a recall on various mobile x-ray units (Optima...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Is-anti-Sm test kits****Catalog No: 720-240*** Product Usage: The...
The Issue: Diamedix Corporation recalled their Is-anti-Sm Test Kit due to the Positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.