Local healthpharmaciesTop News Remedica widens Clonotril recall: check your batch number Farmakeia Relevant News Hard to detect, easy to conceal 13 August 2026 Remedica widens Clonotril recall: check your batch number 13 August 2026 Minor held with adult inmates at overcrowded Limassol centre 13 August 2026 newsroom 13 August 2026 FacebookXWhatsAppEmailPrintViber Remedica Limited is extending its voluntary recall of pharmaceutical products, first announced on August 10, 2026, to cover two additional batches of Clonotril 2mg Tablets. In a clarifying announcement dated August 13, the company confirmed that the following batch numbers have been added to the recall list: 126382 and 126383. The latest update does not include any other pharmaceutical product or any further change to the original list. For all other batches and preparations, the announcement issued on August 10 remains in force. Remedica stresses that the measures taken for all recalled batches are precautionary in nature. The original announcement had clarified that the recall was decided due to certain out-of-specification results in the products’ stability studies, with no cause for concern at this stage. Stability studies are carried out to determine whether a medicine maintains its intended quality characteristics throughout its shelf life when stored under the specified conditions. The new announcement does not provide further information on the test results, nor does it specify why the two additional Clonotril batches were added. Do not stop treatment without medical guidance The company is urging patients that treatment with products from the affected batches should not be discontinued without prior medical guidance. Patients who have packaging bearing one of the recalled batch numbers are asked to contact their treating doctor, who will advise on the most suitable option for safely continuing their treatment. No arbitrary change of medication or dosage should be made, as abruptly stopping certain treatments may carry risks. Replacing the preparation must be decided by a healthcare professional, according to each patient’s individual needs. Citizens can find the batch number on the medication’s packaging and, if it appears on the recall list, should seek instructions from their doctor or pharmacist. Remedica said the decision forms part of the actions it is taking to safeguard patient safety and maintain the trust of its partners. Read more: Overnight pharmacies on Thursday, August 13 Subscribe to our Newsletter Latest News Hard to detect, easy to conceal Minor held with adult inmates at overcrowded Limassol centre Cyprus swelters under yellow heat warning, but the mountains are getting a taste of rain How climate change and El Niño supercharged Typhoon Dolphin Iran says no progress on reviving interim peace deal with US Cyprus banks on AI to boost tourism competitiveness Consumer group doubts Cyprus fuel prices are justified Follow en.philenews on Google News and be the first to know all the news about Cyprus and the world.
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