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Find alerts and recalls issued by MHRA
UKHSA and MHRA are urging the public not to use 4 specified non-sterile alcohol-free wipe products due to the risk of infection associated with their use.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
Sandoz Ltd. have informed the MHRA that the Patient Information Leaflet included in specified batches of Apixaban does not contain up‑to‑date information.
Bio Products Laboratory Limited is recalling one batch of Human Rabies Immunoglobulin following a stability failure for this batch. The batch has shown a reduction in potency of the Human Rabies immunoglobulin.
Summary of the latest safety advice for medicines and medical device users
List of field Safety Notices for 23-27 March 2026
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
New partnership accelerates NHS patients' access to new medicines and will see UK benefit from greater life sciences industry investment.
List of Field Safety Notices for 30 March - 3 April 2026
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