FDA Issues Warning for Defective AEDs
WASHINGTON (MedPage Today) The FDA is warning of potential malfunctions in some 300,000 defibrillators manufactured by Cardiac Science Corporation which may prevent the devices from delivering lifesaving shocks but don’t show up on device self-tests.
source : www.medpagetoday.com
Related News:
- ACOG Issues Guidance Against Surgical Errors
- AAP Issues Statement on Cochlear Implants
- Bleeding Issues with Newer LVADs
- Hastings Center Synthetic Biology Project Raises Moral Issues
- WHO issues warning about corruption of pharmaceutical industry
- AAN: No Pregnancy Issues in Early Natalizumab Review
- Home SpermCheck Test Helps Couples Hoping To Conceive Better Understand Infertility Issues
- After horrible deaths caused by medical radiation mistakes are uncovered, medical group issues (sort of) an apology
- Administration Issues Mental Health Parity Rule
- Johnson & Johnson Issues ‘Massive’ Recall of Tylenol and Motrin Products
Details :
Submited at Friday, November 20th, 2009 at 1:00 pm on Cardiology by ethan
Comment RSS 2.0 - leave a comment - trackback
Leave Comment Here...