AAFES RECALL  NO. 09-062 RELEASE DATE: 17 June, 2009 SUBJECT: QA HAZARDOUS RECALL – Matrixx Initiatives Inc. recalls certain Zicam cold remedies

Scope: Worldwide Matrixx Initiatives Inc. in conjunction with the FDA is voluntarily recalling 3 Zicam cold remedy products marketed for over-the-counter use. AAFES only sold 2 of the 3 products, see product details below. The U.S. Food and Drug Administration advises consumers to immediately stop using the products described below. ITEM DESCRIPTION UPC ZICAM COLD NASAL GEL PUMP 732216010121 ZICAM ADULT NASAL SWAB 732216201017 Hazard: The use of these products is associated with the loss of sense of smell (anosmia). Anosmia may be long lasting or permanent. Incidents/Injuries: The FDA has received more than 130 reports of loss of smell associated with the use of these three Zicam products. Sold At: AAFES facilities worldwide Remedy: Customers should stop using the affected product immediately and contact Matrixx directly at: 1-877-942-2626 or visit the following website: www.zicam.com for more information. Affected products may also be returned to any AAFES retail facility. Click here to view the complete FDA news release. Home | History | About AAFES | Store Locator Contact AAFES | Employment | AAFES Sale Flyers | Online Shopping