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25 lip 2009 · On June 16, 2009, the U.S. Food and Drug Administration (FDA) alerted consumers and members of the healthcare community to discontinue the use of three Zicam Cold Remedy products. In the FDA’s warning letter, they also warned the makers of Zicam to stop selling the defective products.
In June the U.S. Food and Drug Administration issued a warning about some Zicam products based on having received over 130 reports of a decreased sense of smell, often after single use of one of these products. The FDA's action against a homeopathic drug presents a bizarre situation.
1 paź 2024 · The list below provides information gathered from press releases and other public notices about certain recalls of FDA-regulated products. Not all recalls have press releases or are posted...
16 cze 2009 · The Food and Drug Administration is warning consumers not to use three Zicam intranasal products that contain zinc, after receiving 130 reports of anosmia and the loss of sense of smell.
5 wrz 2023 · There are currently no homeopathic products approved by FDA. On December 6, 2022, FDA issued a final guidance, Homeopathic Drug Products, that describes the agency’s approach to prioritizing...
The three products are Zicam Cold Remedy Nasal Gel, Zicam Cold Remedy Nasal Swabs, and Zicam Cold Remedy Swabs: Kids Size (a discontinued product). Matrixx Initiatives is the maker of all three products, and the FDA has warned the company that it cannot market them without the agency's approval.
24 cze 2009 · On June 16, the FDA warned Matrixx to stop selling intranasal versions of its zinc-containing Zicam cold remedy after more than 130 reports of people losing their sense of smell after using the...
