Medical Device Recall Management 2025

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A quality issue resulting in a recall is a serious issue for a medical device company. A company’s actions must be commensurate with the risk of such a serious issue. A recall can be a time of great pressure with a need for urgent investigation and actions. It is best to have procedures ready in advance in order to handle all activities in a diligent and compliant manner. Don’t try to figure it out as you go along. Additionally, a recall can trigger a regulatory inspection and enforcement actions. This webinar will cover these possibilities and how you can best prepare for them. A recall is always a difficult situation but having good procedures and processes in place can help you do the ri...ght thing to protect your customers. This webinar can help you ensure you are ready in the event of a recall-initiated, for-cause inspection. You will understand the regulatory requirements for dealing with a medical device recall. You’ll learn about FDA expectations and regulations as well as lessons learned from 483s and warning letters. We’ll discuss how you can develop your processes to efficiently and effectively manage failure investigations, recalls, and take appropriate corrective and preventive action. In addition, we’ll discuss how to link these processes link to other parts of your Quality Management System. We’ll cover best practices so you can be prepared for a possible post-recall FDA inspection. Mehr lesen