Novo Nordisk Limited would like to notify you of a defect that affects specific batches of NovoRapid FlexTouch prefilled pen device and batches of Saxenda FlexTouch prefilled pen device in the UK. MDR Number MDR 200-05/22 Company name Novo Nordisk
Altan Pharma Limited have identified an error relating to the product packaging. The incorrect concentration of phenylephrine base is provided on the overwrapping bag label. MDR Number MDR 198-05/22 Company name Altan Pharma Limited Product description Phenylephrine 0.08 mg/ml -
Napp Pharmaceuticals Limited have identified an error relating to the Braille printed on the cartons. The Braille message on the Oxycontin 20mg prolonged release tablets incorrectly states strength as 15mg. MDR Number MDR 171-05/22 Company name Napp Pharmaceuticals Limited Product
Orifarm UK have informed us of an error with the Patient Information Leaflet (PIL) packaged within the packs of certain batches. The product name stated in the heading of the PIL has been spelt incorrectly as “lorazolam”, instead of “loprazolam”.
GlaxoSmithKline UK Ltd have informed the MHRA that an incorrect version of the Summary of Product Characteristics section 4.2 and the Patient Information Leaflet is inside the sealed pack, and contains unapproved text. MDR Number MDR 191-03/22 Company name GlaxoSmithKline
Quadrant Pharmaceuticals Ltd are recalling a specific batch of Mefenamic Acid 500mg Film-Coated Tablets as a precautionary measure, due to observations of a defective layer of film coating in some tablets, resulting in the tablet core being partially exposed. MDR
Crescent Pharma Limited are recalling a specific batch of Paroxetine 40mg Film Coated Tablets as a precautionary measure. MDR number MDR 136-03/22 Company name Crescent Pharma Limited Product name Paroxetine 40mg Film Coated Tablets PL 20416/0363 Batch number Expiry date
USV UK Limited are recalling specific batches of products as a precautionary measure due to out of specification results for impurities during routine stability testing. Company name USV UK Limited Product name Olopatadine USV 1mg/mL eye drops, solution PL 32870/0055
Ayrton Saunders Limited have identified an error relating to the Braille printed on the cartons. MDR Number MDR 087-03/22 Company name Ayrton Saunders Limited Product description Careway Hayfever Relief 50 micrograms/dose Nasal Spray PL 16431/0121 Batch Number Expiry Date Pack
Wockhardt UK Ltd are recalling a batch of Diazepam RecTubes 2.5mg Rectal Solution due to an out of specification result for assay during routine stability testing. MDR Number MDR 046-03/22 Company name Wockhardt UK Ltd Product description Diazepam RecTubes 2.5mg