Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, how many patients have reported adverse outcomes following rectopexy mesh procedures in the last ten years; and whether his Department has considered those cases in determining eligibility for mesh-related redress schemes.

Up to and including the 16 March 2026, the Medicines and Healthcare products Regulatory Agency has received a total of 3,303 adverse incident reports. Please note that this search was conducted across all relevant brands, models, and manufacturers associated with the Global Medical Device Nomenclature CT codes listed above and the data is not linked to specific procedures. As such, the data provided will include reports concerning mesh used in a range of different surgical applications, not limited to rectopexy. It is important to note that this data does not directly correlate to the number of United Kingdom procedures undertaken in the UK.

Adverse incident reports are not a direct measure of the number of individual patients affected, as the same incident, or user, may be reported multiple times and duplicates cannot always be reliably linked, and figures may also include cases drawn from published literature and may change slightly as further details are received. Reports may describe recognised complications, and their inclusion does not establish causation or fault with any particular device, so the data should not be interpreted as a summary of known or proven adverse reactions.

The Government is carefully considering the work by the Patient Safety Commissioner and her report, which set out options for redress for those harmed by valproate and pelvic mesh. The abovementioned data will form part of the Department’s considerations regarding a redress scheme.