The Implant Files investigation reveals damage caused by poor regulation and lax testing rules
• Why we’re examining the implants industry
Patients around the world are suffering pain and many have died as a result of faulty medical devices that have been allowed on to the market by a system dogged by poor regulation, lax rules on testing and a lack of transparency, an investigation has found.
Pacemakers, artificial hips, contraceptives and breast implants are among the devices that have caused injuries and resulted in patients having to undergo follow-up operations or in some cases losing their lives.
Related: From orange bags to Essure: why we’re examining the implants industry
Replacement hips and vaginal mesh products sold to hospitals without any clinical trials.
Patients relying on faulty pacemakers when manufacturers were aware of problems.
Complications with hernia mesh that ruled one of Britain’s top athletes out of competing for years.
Regulators approving spinal disc replacements that later disintegrated and migrated in patients.
Surgeons admitting they were unable to tell patients about the risks posed by implants because of a lack of central registers.
Patients in Australia being given devices that the regulator has approved on the basis they have been approved in Europe.
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