Don’t relax over this
ROCKVILLE
,
MD
- MedWatch, the Safety Information and Adverse Event Reporting Program of the U.S. Food and Drug Administration (FDA), and Woodridge Labs told consumers and healthcare professionals of a recall of all DermaFreeze365 Instant Line Relaxing Formula and DermaFreeze365 Neck and Chest products. Certain lots tested positive for Pseudomonas aeruginosa bacteria, which may cause serious eye, urinary tract, bone and joint, respiratory system, and soft tissue infections; dermatitis, bacteremia, gastrointestinal and other systemic infections, particularly in those with severe burns and in cancer and AIDS patients who are immuno-suppressed. Because DermaFreeze365 Instant Line Relaxing Formula may be applied in the eye area, there is a chance that if the recalled product is inadvertently put in the eye, it could bring serious eye infections and, sometimes, possible blindness. Read the complete MedWatch Safety summary at www.fda.gov/medwatch/safety/2007/safety07.htm#DermaFreeze365.
