To ask the Secretary of State for Health and Social Care, how many manufacturers, distributors and importers of e-cigarette products provided data on any adverse effects linked to their products, following the request for that data by the Medicines and Healthcare products Regulatory Agency in October 2019; and what proportion that accounted for of all notified e-cigarettes and refill containers.
To ask the Secretary of State for Health and Social Care, what enforcement action he has taken against (a) manufacturers, (b) distributors and (c) importers of e-cigarette products for alleged non-compliance with Article 39 vigilance requirements in the Tobacco and Related Products Regulations 2016 and non-reporting of adverse effects in relation to their products, since the October 2019 request by the Medicines and Healthcare products Regulatory Agency.
In October 2019, in light of the emerging suspected cases of e-cigarette or vaping associated lung injury in the United States, the Medicines and Healthcare products Regulatory Agency (MHRA) requested data from 513 producers of nicotine containing e-liquid listed on the United Kingdom notified products list. The request was for information relating to any suspected respiratory adverse reaction in association with their products.
Overall 275 responses were received, covering approximately 72% of notified products. Seventeen producers confirmed they had received reports and provided data. This resulted in the addition of 125 cases of adverse respiratory reactions to the MHRA database of suspected adverse reaction reports to e-cigarette products.