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Commons Briefing paper by Claire Duddy. It was first published on Thursday, 5 February 2026. It was last updated on Friday, 20 February 2026.


Pelvic mesh and sodium valproate

Pelvic mesh and sodium valproate are two medical products that are known to have caused harm to many patients.

Both were considered by the Independent Medicines and Medical Devices Safety Review (the Cumberlege review). The review also considered the hormone pregnancy test, Primodos. The Library briefing Hormone pregnancy tests provides more information about these medicines.

Pelvic mesh and sodium valproate

Mesh is a medical device that can be surgically implanted into the body to support organs and other tissues. Pelvic mesh (also known as vaginal mesh) has been commonly used in the treatment of stress urinary incontinence (the involuntary leaking of urine during effort or exertion) and pelvic organ prolapse (when body organs in the pelvis move out of position and bulge into the vagina). Pelvic mesh can cause a range of complications, including erosion (when mesh breaks down in body tissues), protrusion of mesh into the vagina or other organs, pain, urinary problems, infection and bleeding.

Sodium valproate is a medicine that is used to treat epilepsy and bipolar disorder. It is known to cause foetal abnormalities when it is used during pregnancy, including neurodevelopmental disorders and congenital malformations (birth defects).  

The Independent Medicines and Medical Devices Safety Review (Cumberlege review)

The Independent Medicines and Medical Devices Safety (IMMDS) review published its final report, First Do No Harm, in July 2020. It made nine recommendations, including that the government should establish an independent redress agency and specific redress schemes for patients harmed by pelvic mesh and sodium valproate.

The government did not accept the report’s recommendations in relation to redress, but in December 2022, it announced that it had asked the Patient Safety Commissioner (for England) to explore options for a redress scheme for people affected by sodium valproate and mesh.

The Patient Safety Commissioner (Dr Henrietta Hughes) agreed terms of reference for the PSC Redress Project in Spring 2023 and work began in Summer 2023.

The Hughes Report

On 7 February 2024, the Patient Safety Commissioner published The Hughes Report, setting out further recommendations for redress for those harmed by sodium valproate and pelvic mesh. The report calls for the establishment of an independent two-stage redress scheme to provide both financial and non-financial redress for affected patients. 

The government has not yet responded to the report. It has repeatedly stated that it is carefully considering the report and its recommendations.

In a debate to mark the second anniversary of the report’s publication, on 11 February 2026, the government was asked about the delay in responding to the report. It said that it was “committed to setting out our response at the earliest credible opportunity while ensuring that it is both robust and deliverable”.

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Secondary information

Type
Research briefing
Reference
CBP-10487 
Related items
Hughes Report: Second Anniversary
Wednesday, 11 February 2026
Parliamentary proceedings
House of Commons
Subjects
Compensation Patients Medicines and Medical Devices Safety Independent Review Foetal valproate spectrum disorder Patient Safety Commissioner Primodos Sodium valproate Surgical mesh implants Pregnancy tests
Published by
Science and Environment Section
House of Commons Library
Link
View this Research briefing on researchbriefings.parliament.uk