| Subject: | FDA Issues Public Health Notification on Unretrieved Device Fragments |
| Category: | Food and Drug Administration (FDA)
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| Published: | Thu, 17 Jan 2008 - 06:00 am |
| Audience: Radiologists, surgeons, hospital risk managers, other healthcare professionalsThe FDA is advising healthcare professionals of serious adverse events associated with unretrieved device fragments (UDFs). A UDF is a fragment of a medical device that has separated unintentionally and remains in the patient after a procedure. Patients may not be aware that this has occurred. The FDA Center for Devices and Radiological Health receives nearly 1000 adverse event reports each year related to... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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