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FDA orders immediate recall of alcoholic energy drinks from markets

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The review examined both the health implications and regulatory compliance status

The Food and Drugs Authority (FDA) has ordered the immediate withdrawal of alcoholic beverages blended with stimulants from the Ghanaian market, setting a compliance deadline of March 31, 2026.

The directive, contained in a press statement issued on February 25, 2026, targets products that combine alcohol with ingredients such as caffeine, inositol, glucuronolactone, ginseng, and guarana.

According to the Authority, the action follows a post-registration safety review conducted under Sections 81 and 82(a) of the Public Health Act, 2012 (Act 851).

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“The review examined both the health implications and regulatory compliance status of such beverages, while also considering evolving international standards,” the statement said.

The FDA noted that several countries have already restricted or banned alcoholic energy drinks due to growing public health concerns.

https://www.ghanaweb.com/GhanaHomePage/business/FDA-issues-immediate-recall-of-Grand-Chateaux-Sangria-Forte-over-safety-legality-concerns-1976261

It cited scientific findings that indicate that mixing alcohol with stimulants can heighten health risks and encourage adverse behavioural patterns, especially among young people.

The stimulant elements, the Authority explained, may reduce the perception of intoxication, increasing the likelihood of overconsumption and adverse behaviour.

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The evaluation was carried out with support from the FDA’s Food Expert Committee and the Technical Advisory Committee on Food Safety and Nutrition.

Manufacturers have been instructed to reformulate affected products in line with approved standards, ensuring that alcoholic beverages and energy drinks are marketed as distinct product categories.

The Authority cautioned that failure to comply by the stipulated deadline will attract regulatory sanctions, including enforced withdrawal from the market.

Reiterating its mandate to protect public health, the FDA called on the public to remain alert and report any non-compliant products for swift action.

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Read the full statement below

MRA/VPO

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Source:
www.ghanaweb.com

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