Nigerian Public Alert 82: The National Agency for Food and Drug Administration and Control (NAFDAC) is informing the public of the detection of suspected counterfeit medicinal products found in the Nigerian market that infringe on the approved marketing authorization of Forxiga® (dapagliflozin) manufactured by AstraZeneca.
Category: Admin: Public Alerts
Nigerian Public Alert 81: NAFDAC Notifies on Marketing and Sale of Unregistered Menofix Composition
Nigerian Public Alert 81: The National Agency for Food and Drug Administration and Control (NAFDAC) is alerting the public about the marketing and sale of unregistered Menofix Composition.
Nigerian Public Alert 80: NAFDAC Notifies on Niger Republic Imposing Import Ban on Bulmex Parboiled Rice from India due to Metallic Contamination
Nigerian Public Alert 80: The National Agency for Food and Drug Administration and Control (NAFDAC) has been informed that the Niger Republic’s Ministry of Trade and Industry has banned the importation of Bulmex Parboiled Rice from India.
Nigerian Public Alert 79: NAFDAC Notifies on Voluntary Recall of Sporidex Suspension 125 mg/5 ml (Batch No. DFG4606A)
Nigerian Public Alert 79: The National Agency for Food and Drug Administration and Control (NAFDAC) is notifying healthcare providers and the public of the voluntary recall of Sporidex Suspension 125 mg/5 mL, Batch No. DFG4606A.
Nigerian Public Alert 78: NAFDAC Notifies on Confiscation of a Banned Alcoholic Energy Drink in Ghana
Nigerian Public Alert 78: The National Agency for Food and Drug Administration and Control (NAFDAC) received a notification that the Ghana Food and Drugs Authority confiscated approximately 140 boxes of a banned alcoholic energy drink found in circulation in the Upper East Region of Ghana.
Nigerian Public Alert 77: NAFDAC Notifies on Recall of Sexual Enhancement Product Due to Undeclared Pharmaceutical Ingredients
Nigerian Public Alert 77: The National Agency for Food and Drug Administration and Control (NAFDAC) received a notification that Best Supplements Best Prices Company is voluntarily recalling all lots of WAP Sensual Enhancement capsules to the consumer level following the detection of undeclared pharmaceutical ingredients by the U.S Food and Drug Administration.
Nigerian Public Alert 76: NAFDAC Notifies on Withdrawal of Levamisole-Containing Medicines as endorsed by the Italian Medicines Agency (AIFA) over serious Neurological risks
Nigerian Public Alert 76: The National Agency for Food and Drug Administration and Control received a notification that on 6 April 2026, the Italian Medicines Agency (AIFA) endorsed a safety recommendation to withdraw medicines containing levamisole from the EU market.