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. 2,562 recalls have been distributed to Oregon in the last 12 months.
Showing 16381–16400 of 28,488 recalls
Recalled Item: ZMS Intramedullary Fixation Smooth Guide Wire 2.4 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mutlidiagnost-Eleva with Flat Detector Eleva with Flat Detector 708037 As...
The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 708033 URODiagnost As a multifunctional universal imaging application system...
The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visualase Cooled Laser Applicator System (VCLAS) labeled as: a. Part...
The Issue: Medtronic has become aware that certain lots of the VCLAS 3MM, 10MM, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann¿ Emdogain 0.3 ml Multipack USA. Enamel Matrix Derivative. Article...
The Issue: A change regarding the shelf life of a raw material was implemented without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann¿ Emdogain 015 Recalled by Straumann Manufacturing, Inc. Due to A...
The Issue: A change regarding the shelf life of a raw material was implemented without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic ZEVO(TM) Anterior Cervical Plate System SLOT SCREW Recalled by...
The Issue: Slot screw had an overall length of 15mm, but per the specification, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann¿ Emdogain 0.7 ml Multipack USA. Enamel Matrix Derivative. Article...
The Issue: A change regarding the shelf life of a raw material was implemented without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann¿ Emdogain 0.3 ml Multipack. Enamel Matrix Derivative. Article...
The Issue: A change regarding the shelf life of a raw material was implemented without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann¿ Emdogain 0.7 ml Multipack. Enamel Matrix Derivative. Article...
The Issue: A change regarding the shelf life of a raw material was implemented without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann¿ Emdogain 0.15 ml 5-Pack. Enamel Matrix Derivative. Article Number...
The Issue: A change regarding the shelf life of a raw material was implemented without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E90 ultrasound system Product Usage: Vivid E80 / Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE LOGIQ E9 ultrasound system Product Usage: The device is Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E95 ultrasound system Product The device is intended Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E80 ultrasound system Vivid E80 / E90 / Recalled by GE Medical...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid 7 ultrasound system Product Usage: Vivid E7 is Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE LOGIQ 9 ultrasound system Product Usage: The device is Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Lithium Heparin Green Top Tube Recalled by Becton Dickinson &...
The Issue: BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E9 ultrasound system Product Usage: GE Vivid E9 Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ EDTA Pink Top Tube Recalled by Becton Dickinson & Company Due...
The Issue: BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.