Infusion Pump Recall: Zyno Medical Removes Certain Z-800 Series Infusion Pumps due to Software Issue

The Food and Drug Administration is advising consumers not to purchase or use VITAFER-L Gold 20ml, a product promoted for energy and sexual enhancement on various websites, including www.amazon.com.

CGMP/Finished Pharmaceuticals/Adulterated

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program.

Olympus is removing certain High Flow Insufflation Unit models due to software issues that may lead to overpressure events.

FDA 483, dated June 11, 2008, (9 pages)

Unapproved New Drugs/Misbranded