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. 2,635 recalls have been distributed to Oregon in the last 12 months.
Showing 10481–10500 of 28,488 recalls
Recalled Item: VITROS Chemistry Products CKMB Slides: (1)VITROS CKMB Slides (60 Slide...
The Issue: VITROS Chemistry Products CKMB Slides Potential for Falsely Elevated Results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 600FP Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has become aware of a potential safety issue associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...
The Issue: Due to a manufacturing error their is a potential that the sheath within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...
The Issue: Due to a manufacturing error their is a potential that the sheath within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...
The Issue: Due to a manufacturing error their is a potential that the sheath within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...
The Issue: Due to a manufacturing error their is a potential that the sheath within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...
The Issue: Due to a manufacturing error their is a potential that the sheath within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TLAB Recalled by Argon Medical Devices, Inc Due to Due...
The Issue: Due to a manufacturing error their is a potential that the sheath within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clerio Vision Recalled by Clerio Vision Due to One lot of contact lenses...
The Issue: One lot of contact lenses labeled as BC MED, DIA 14.0 PWR -2.25 contained BC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoTherapy Treatment Delivery System with iDMS - Product Usage: used...
The Issue: "MLC tickle error" may result in the delivered dose to effectively rotate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoTherapy Treatment System - Product Usage: used as an integrated Recalled...
The Issue: "MLC tickle error" may result in the delivered dose to effectively rotate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000F Catheterization...
The Issue: System table may tilt because the bolts that fasten the vertical column and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000C Catheterization...
The Issue: System table may tilt because the bolts that fasten the vertical column and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000V Catheterization...
The Issue: System table may tilt because the bolts that fasten the vertical column and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 Image-intensified fluoroscopic x-ray system Recalled by...
The Issue: After the user selects the Lock-in command, the kV and mA values are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC-107: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-108: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC-108: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix" PMIC-109: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ares Antibiotic-Impregnated Catheter Recalled by Medtronic...
The Issue: There is a potential for a defect on the seal of the outer pouch of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.