Delaware Handbook: Medical Products Recalls HOW WILL WE KNOW IF A DRUG OR A PRODUCT WE USE IS RECALLED? Occasionally, drugs and medical products are recalled or become the subject of “safety alerts” issued by the U.S. Food and Drug Administration (FDA). Medical practices often receive calls from patients who hear about such events on the news or read about them on the Internet. If you have not heard about the recall and a patient brings the issue to your attention, you first must determine whether the product really has been reca... Are you a Curi member? The full content of this resource is available only to Curi members. Contact us if you are a member but do not have an account yet, or to learn more about becoming a Curi member. Sign in to see full post News & Knowledge READ NEXT January 13, 2023March 9, 2023Clinical Care | Patient Management | Patient Satisfaction | Physician Patient Relationship Guidance for Disclosure of Adverse Events Communicating with patients and families after an unexpected adverse outcome can be difficult. A proactive disclosure of an adverse outcome may defuse anger and prevent potential litigation. Read more July 29, 2022February 15, 2023Clinical Care | Forms & Templates | Patient Management | Policy Templates Policy: Transition of Pediatric Patient to Adult Provider Policy Read more July 29, 2022February 15, 2023Clinical Care | Forms & Templates | Policy Templates Policy: Using Physician Approved Protocols to Refill Medications Policy Read more