Zicam® Recall: SEC & FDA Investigates Matrixx
On June 24, 2009 the Associated Press (AP) reported that the U.S. Food & Drug Administration (FDA) is looking into whether Matrixx Initiatives Inc. unlawfully marketed the Zicam product and the U.S. Securities & Exchange Commission (SEC) has launched a formal investigation of Matrixx Initiatives Inc.
These investigations follow the June 16, 2009 Zicam and loss of smell warning letter from the FDA, which resulted in the company recalling a variety of Zicam products.
Matrixx has settled hundreds of lawsuits connected with Zicam in recent years, though it maintains the nasal spray does not harm users’ sense of smell.
Zicam Recall List
The following products have been recalled by Matrixx after the FDA linked them to a large number of consumer injury reports regarding the use of the products and the subsequent loss of smell, also known as Anosmia.
- Zicam Cold Remedy Nasal Gel
- Zicam Cold Remedy Nasal Swabs
- Zicam Cold Remedy Swabs, Kids Size (a discontinued product)
Do I Have a Zicam Loss of Smell Lawsuit?
The Schmidt Firm, LLP is currently accepting Zicam induced anosmia claims in all 50 states. If you or somebody you know has taken Zicam and suffered from the loss of sense of smell, or anosmia, you should contact our firm immediately for a free case consultation. Please click here to contact our Dangerous Drug Litigation Group, use the form below or call toll free 24 hours a day at (866) 920-0753.
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