Brown & Burk UK Limited have noticed an error regarding specific batches of Amoxicillin 500 mg/ 5 ml Powder for oral suspension. The product information incorrectly states the quantity of the excipient sodium benzoate. PL Number PL 25298/0248 MDR Number
Napp Pharmaceuticals Limited have noticed and an error in the PIL of specific batches of Sevredol 10 mg Tablets and Sevredol 20 mg Tablets. PL Number(s) PL 16950/0063, PL 16950/0064 MDR Number MDR 074-07/21 Company Name Napp Pharmaceuticals Limited Product
Galderma UK identified an error regarding an older version of artwork being used and packed with specific batches of Tetralysal 300mg Hard Capsules. PL Number(s) PL 10590/0019 MDR Number MDR 387-06/21 Company Name Galderma UK Product description Tetralysal 300mg Hard
CLMR Number CLMR (21)A/05 MDR Number MDR 377-06/21 Company Name Nova Laboratories Limited (MS 13581) Product description Morphine Syringe 50mg/50ml (unlicensed medicine) Magnesium Sulphate 8mmol/20ml infusion (unlicensed medicine) Lot Number/Expiry Product name Batch Number Expiry Date Pack Size First Distributed
In May 2021 CQC released guidance around culturally appropriate care. We have designed an Equality & Diversity Audit which covers the key themes of this guidance and blended this with requirements around accessible information standards to ensure that Culturally appropriate
Specific batches of products supplied by Bristol Laboratories Limited, Brown & Burk UK Limited and Teva UK Limited are being recalled due to presence of a mutagenic impurity. Company name Bristol Laboratories Limited Irbesartan 75 mg Film Coated Tablets, PL
Recall of Co-codamol 30/500 Effervescent Tablets, Batch 1K10121, Zentiva Pharma UK Ltd due to precautionary risk of causing overdose Zentiva Pharma UK Limited have notified the MHRA of an issue related to the homogeneity of a batch of Co-codamol 30/500
This Induction Booklet is designed to support in the Induction of Care Workers who are joining your team. The document will be available to download as a Word (editable) document. Regulation 18 of the Health & Social Care Act (Regulated
Advanz Pharma is recalling batches of carbimazole tablets due to an out of specification observation for tablet appearance of samples during routine stability testing. PL Number(s) PL 20072/0244 PL 20072/0245 MDR Number MDR 359-04/21 Company Name Advanz Pharma Product description
CQC and local authorities will ask for Provider records of visits. We have developed a Provider visit report template that can be used to evidence Provider oversight and governance of a service. The template covers; Discussions with service users, staff,