Matrixx failed to give 800 Zicam reports to FDA

by Michael J. Evans on June 23, 2009

in Consumer Protection,Dangerous Products

Bloomberg is reporting that Maatrixx, the manufacturer of Zicam nasal spray and swabs, didn’t give the FDA 800 complaints it received about side-effects of the recalled products.  The products were recalled June 16 after the Food and Drug Administration warned consumers that the treatments may cause a loss of smell.

Share

Comments on this entry are closed.

Previous post:

Next post: