Kenya’s PPB detects falsified Lucentis batches 18862110 and 18802112
The Pharmacy and Poisons Board has identified two falsified batches of Lucentis (ranibizumab) 0.3mg injection in the Kenyan market, with one arrest made and…
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Recalls, falsified medicines, agency alerts and import holds — with batch numbers.
Showing 1–11 of 11 notices
The Pharmacy and Poisons Board has identified two falsified batches of Lucentis (ranibizumab) 0.3mg injection in the Kenyan market, with one arrest made and…
Read the notice →The Agence Marocaine du Médicament et des Produits de Santé has recalled two batches of Cardioaspirine 100 mg gastro-resistant tablets after a temperature deviation…
Read the notice →Steris Verify Dual Specific Self-Contained Biological Indicators for Steam and ETO (S3060) are being recalled in South Africa by SafMed…
Read the notice →Two lots of the BiCOAG Hemostasis Probe are being recalled in South Africa after Olympus, the original equipment manufacturer, determined…
Read the notice →Nigeria’s National Agency for Food and Drug Administration and Control (NAFDAC) has alerted the market to four batches of medicines…
Read the notice →The Egyptian Drug Authority (EDA) has ordered a Class II recall of one batch of Vilaphoria 40mg film-coated tablets, manufactured…
Read the notice →The Egyptian Drug Authority (EDA) has ordered a Class I recall of one batch of Appavisc HVPFS, manufactured by Chironephre…
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South Sudan recalls Duphaston and Navidoxine over quality and falsification concernsSouth Sudan’s Drug and Food Control Authority (DFCA) has ordered…
Read the notice →Nigeria’s National Agency for Food and Drug Administration and Control (NAFDAC) has warned that suspected falsified products imitating Forxiga (dapagliflozin)…
Read the notice →Post-marketing surveillance found out-of-specification results in the hypertension medicine; the Class II recall covers four batches of 28-tablet packs, two of which remain in…
Read the notice →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…
Read the notice →Independent pharmaceutical news and regulatory intelligence covering Africa.