In a recent announcement, the Food and Drugs Authority (FDA) has notified the public regarding the recall of Benylin Paediatric (100mls) Syrup, LOT No. 329304, by the Nigerian National Agency for Food and Drugs Administration (NAFDAC). Manufactured by Johnson & Johnson (Pty) in South Africa. This cough mixture has been found to contain an “unacceptably high level” of diethylene glycol (DEG), a poisonous substance to humans.
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DEG ingestion can cause severe health issues, including headaches, abdominal pain, vomiting, diarrhea, paralysis, convulsions, acute kidney failure, and difficulty urinating, with potentially fatal consequences.
The FDA confirms LOT No. 329304 is not on the Ghanaian market yet but it is taking prevention measures by intensifying surveillance at all entry ports . Since 2022, all imported syrup formulations undergo DEG testing. Other lots of Benylin Paediatric 100mls syrup in Ghana tested negative for DEG.
The public is urged to report any sightings of the affected syrup to FDA offices across Ghana. For further information, contact the FDA via their website www.fdaghana.gov.gh, or call 0551112224/5, or email at fda@fda.gov.gh. Also on social media platforms Instagram and Twitter (@fdaghana), and Facebook (fdaghana).
This cautionary announcement aims to ensure the safety and well-being of the public amidst concerns over the contaminated product.
Source: Senam Joanita Amegashie
