Profession
FDA: Device fragments can harm patients
NEWS IN BRIEF — Posted Feb. 11, 2008
More than 1,000 adverse events involving medical device fragments left inside patients are reported to the U.S. Food and Drug Administration each year, the agency said in a warning to doctors and other health care professionals last month.
Unretrieved device fragments can lead to serious injury and death, the FDA said.
Note: This item originally appeared at http://www.ama-assn.org/amednews/2008/02/11/prbf0211.htm.












