ANPP recalls one batch of Arovan atorvastatin over quality defect
The Agence Nationale des Produits Pharmaceutiques has ordered a batch recall of Arovan atorvastatin 10 mg tablets after identifying a quality defect; the affected…
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Alerts & Recalls
Recalls, falsified medicines, agency alerts and import holds — with batch numbers.
Latest in Alerts & Recalls
Showing 1–8 of 8 notices
ANPP quarantines eight batches of Clamoxyl amoxicillin over quality defect
The Agence Nationale des Produits Pharmaceutiques has imposed a quarantine on eight batches of Clamoxyl 1g amoxicillin tablets after identifying a quality defect.
Read the notice →ANPP recalls one batch of Isotanak ginkgo biloba oral solution over quality defect
The Agence Nationale des Produits Pharmaceutiques has ordered a batch recall of Isotanak ginkgo biloba oral solution after identifying a quality defect; the affected…
Read the notice →ANPP recalls one batch of Ferolam sodium feredetate syrup over quality defect
The Agence Nationale des Produits Pharmaceutiques has ordered a batch recall of Ferolam sodium feredetate syrup after identifying a quality defect; the affected batch…
Read the notice →ANPP recalls one batch of GANT H surgical gloves over quality defect
The Agence Nationale des Produits Pharmaceutiques has ordered a voluntary batch recall and quarantine of GANT H sterile latex surgical gloves, size 6.5, after…
Read the notice →BoMRA announces voluntary recall of eight Remedica medicines
The Botswana Medicines Regulatory Authority has notified the public of a voluntary recall of 35 batches of eight medicines manufactured by Remedica Limited and…
Read the notice →BoMRA recalls Flumed Syrup batch after crystallisation found
One batch of the paracetamol-based combination cough and cold syrup, made by Varichem Pharmaceuticals of Zimbabwe, has been recalled from the Botswana market.
Read the notice →Somaliland suspends sale of YENISOM medicines over missing quality testing
The order covers YENISOM Healthcare's entire range rather than named batches, and the agency says the ground is procedural: required entry testing was not…
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Independent pharmaceutical news and regulatory intelligence covering Africa.