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The consumer healthcare company is recalling the cough syrup, sold under the brand name "Robitussin Honey CF Max Day Adult" in 4-ounce and 8-ounce doses, along with its 8-ounce night-time version.
This list is not limited to drugs that were ever approved by the FDA. Some of them (lumiracoxib, rimonabant, tolrestat, ximelagatran and ximelidine, for example) were approved to be marketed in Europe but had not yet been approved for marketing in the US, when side effects became clear and their developers pulled them from the market.
OTC, prescription, and compounded drugs (drugs tailored to a specific patient) each pose unique challenges to the recall process. Over the counter drugs are widely distributed and there is no direct link between company and consumer. Recalls are typically only advertised online and in the media, so consumers are subject to their own awareness.
The recalled medicine is Kirkland Signature brand's "Severe Cold and Flu Plus Congestion" medication, sold between Oct. 30 and Nov. 30, 2024. The recalled items have a Lot Code of P140082 on the box.
The company markets over-the-counter and prescription medical products including complete lines of Tylenol and Motrin IB products for adults and children. [citation needed] The company is located in Fort Washington, Pennsylvania, and employs 2,600 people. [citation needed] Annual sales in 2004 were US $2.1 billion.
If you have questions regarding the recall, you can contact Alcon Laboratories at 1-800-241-5999 between 7:30 a.m. and 6:00 p.m. CST between Monday and Friday. If you have concerns regarding a ...