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Neon Healthcare Ltd is recalling the specific batch mentioned in this notification as a precautionary measure.
The MHRA was alerted by Beyond Compliance and the UK National Joint Registry (NJR) to a significantly higher revision rate observed with the ORIGIN PS patient-matched total knee replacement.
Employment Appeal Tribunal Judgment of Lord Fairley on 18 April 2024.
Bristol-Myers Squibb Pharmaceuticals Limited has informed the MHRA that a potential product quality issue has been detected, relating to incomplete crimping of the metal crimp cap of OPDIVO 10mg/mL concentrate for solution for infusion (nivolumab) (1VLX10ML).
You must have a legacy-proofing plan for all digital services to prevent the build up of technical debt and future legacy
Check if you need a tuberculosis (TB) test to support your visa application and find an approved clinic in your country
Check the tariff classification for peptide nisin standardised with sodium chloride
Product Safety Report for High voltage string lights, HM-E12-1(25) sold via Amazon presenting a high risk of fire.
Fresenius Kabi Limited has informed the MHRA of an error on the infusion bag packaged into the specific batches of Sodium Chloride Intravenous Infusion 0.9% Freeflex.
medac GmbH (t/a medac Pharma LLP) is recalling the product for the batch specified in this notification due to particles detected during long-term stability tests.
Information for HM Passport Office staff about countries and territories beginning with the letters T to Z.
Keep up to date with the UK policy development in respect of Standard Essential Patents.
Check the tariff classification for the unassembled parts to be implanted into the human body for different spinal treatments.
Product Recall for Hisea Life Jacket presenting a serious risk of drowning.
Information for clinicians on diagnosis and notification of Shiga toxin-producing Escherichia coli (STEC) and haemolytic uraemic syndrome (HUS).
Crescent Pharma Limited has informed the MHRA regarding an error with the European Article Number (EAN) barcode on the cartons of the above-mentioned batches of Pantoprazole 40 mg Gastro-Resistant Tablets distributed by Crescent Pharma Limited.
Report certain types of medical conditions to DVLA if you're a lorry, bus or coach driver.
Information and guidance for verifying your identity.
Accord-UK Ltd is recalling a specific batch of Co-Codamol 8/500mg Effervescent Tablets (Key Pharmaceuticals Livery) as a precautionary measure due to the internal tablet blister strips being printed with an incorrect expiry date.
Product Recall for Black and Yellow Sporting Harness sold via Fruugo presenting a serious risk of injuries.
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