The Medicines Control Authority of Zimbabwe (MCAZ) has taken immediate action to recall Benylin Paediatric Syrup over fears of potential toxic batches infiltrating the Zimbabwean market.

In a statement released on Monday, MCAZ explained that the decision was a precautionary measure following the recall of the product in Nigeria and several other countries.

The National Agency for Food and Drug Administration (NAFDAC) of Nigeria recalled batch number 329304 of Benylin Paediatric 100ml syrup, manufactured by Johnson and Johnson, South Africa. Additionally, the South African Health Products Regulatory Authority (SAHPRA) and the manufacturer identified another affected batch, bringing the total to two – 329303 and 329304.

“While the Authority confirms the registration of this product in Zimbabwe in 2023, our import database does not show records of these specific batches being imported. However, there is concern that these batches may have entered the local market through illegal means,” MCAZ stated.

NAFDAC’s recent laboratory analysis revealed dangerously high levels of Diethylene glycol in the syrup, a toxic contaminant when consumed by humans. Toxic effects can include abdominal pain, vomiting, diarrhea, altered mental state, and acute kidney injury, potentially leading to death.

MCAZ urged the public to report any possession or encounter with the blacklisted product and advised against administering the recalled medicine to children.

In the meantime, MCAZ announced plans to conduct strict surveillance through premises inspections and public awareness initiatives.