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. 2,470 recalls have been distributed to Oregon in the last 12 months.
Showing 24881–24900 of 28,488 recalls
Recalled Item: PRE2001: Prevena Incision Management Customizable System Box Product Usage:...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE1001: Prevena Peel and Place System Kit Product Usage: The Recalled by...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE2001US: Prevena Incision Management Customizable System Box (US-ONLY)...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE1055US: Prevena Dressing Recalled by KCI USA, INC. Due to Prevena...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Select CAP Arterial Cannulae. Vented Recalled by Medtronic Inc....
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes CMF Battery Powered Driver Recalled by Synthes, Inc. Due to The CMF...
The Issue: The CMF Battery Powered Driver graphic case contains outlines of the Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Intersept Custom Tubing Pack which contain Select 3D or Recalled...
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Select 3D Arterial Cannulae. Vented Recalled by Medtronic Inc....
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Select 3D Arterial Cannulae. Vented Recalled by Medtronic Inc....
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Select CAP Arterial Cannulae. Non-Vented Recalled by Medtronic...
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gelzone Shoulder Sleeve Recalled by Implantech Associates Inc Due to...
The Issue: Implantech initiated the voluntary recall of Gelzone Shoulder Sleever,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Certain Silicone TECNIS IOLs may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accessory shorts for the AlterG Anti-Gravity treadmill. Use with the...
The Issue: Unapproved material used by vendor in subset of shorts causing them to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Recalled by Cardiovascular Systems, Inc. Due to Cardio vascular Systems...
The Issue: Cardio vascular Systems Inc. has initiated a recall to request the immediate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 3.2 mm Guide Wire 400mm. Used for guiding the Recalled by Synthes,...
The Issue: Synthes 3.2 mm Guide Wire 400mm included an incorrect raw material listed on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Notch Titanium Reconstructive Plate Product Usage: The Synthes...
The Issue: Certain modules containing the Synthes Small Notch Titanium Reconstructive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Dynamics Picture Archiving and Communication System (PACS). Model...
The Issue: Potential patient data mixup. Improper error handling could allow for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum XL3 Multi line Infusion System Recalled by Hospira Inc. Due to There is...
The Issue: There is the potential for the door roller assembly on the Plum LifeCare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RetCam 3 Recalled by Clarity Medical Systems Inc Due to Software anomaly for...
The Issue: Software anomaly for RetCam 3, RetCam Shuttle and RetCam Portable with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Kodak 2200 Intraoral X-Ray System Recalled by Carestream Health Inc....
The Issue: Carestream received problem reports relating to apparent early failure of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.