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. 2,557 recalls have been distributed to Oregon in the last 12 months.
Showing 17421–17440 of 28,488 recalls
Recalled Item: Platinium CRT-D 1741 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium DR 1510 Recalled by Sorin Group Italia SRL - CRF Due to There is a...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium CRT DF1 1711 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium VR DF4 1240 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX-2 COUDE Epidural Needle Recalled by Epimed International Due to Potential...
The Issue: Potential for partially incomplete seal of product, impacting sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COUDE Blunt Nerve Block Needle Recalled by Epimed International Due to...
The Issue: Potential for partially incomplete seal of product, impacting sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Direct Swish Duo-Grip Healing Collar Recalled by Implant Direct...
The Issue: The Swish Duo-Grip Healing Collar part number 9048-13H (4.8mm) package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FUJINON ED-530XT. This device is intended for the visualization of Recalled...
The Issue: An update to the design and labeling was implemented to help reduce patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPIFE ImmunoFix-6 Kit Recalled by Helena Laboratories, Corp. Due to The...
The Issue: The plates do not have wells punched for the controls in the patient 1 area.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sekisui Diagnostics Sekure Chemistry Acetaminophen L3K Recalled by Beckman...
The Issue: Reagent carryover from Sekisui ACTH when utilized on the BEC AU 680 analyzer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance Scissors Tool Tip The Percutaneous Surgical System with 5mm...
The Issue: For some of the recalled products, the security of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance Gripper Grasper Tool Tip The Percutaneous Surgical System with...
The Issue: For some of the recalled products, the security of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance 29cm Shaft The Percutaneous Surgical System with 5mm attachments...
The Issue: For some of the recalled products, the security of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance Clip Applier Tool Tip The Percutaneous Surgical System with...
The Issue: For some of the recalled products, the security of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance Johans Grasper Tool Tip The Percutaneous Surgical System with...
The Issue: For some of the recalled products, the security of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance Maryland Dissector Tool Tip The Percutaneous Surgical System with...
The Issue: For some of the recalled products, the security of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Elastic Esmark Bandage Recalled by Medline Industries Inc Due to...
The Issue: Product did not undergo correct sterilization procedures and may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas 6000 Modular Series system Recalled by Roche Diagnostics Corporation...
The Issue: A warning is being added to the cobas¿ 6000 MODULAR Series System - c501 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas 8000 Modular Analyzer Series Recalled by Roche Diagnostics Corporation...
The Issue: A warning is being added to the cobas¿ 6000 analyzer and the cobas¿ 8000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife(TM) Reduced Heparin ARTERIAL BLOOD SAMPLER Recalled by Vyaire...
The Issue: Lot #0001047501 of the 9025RHTR ABG sampling kits have been manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.