Medical Device Makers Are Getting a Break From the FDA
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Medical Device Makers Are Getting a Break From the FDA
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The FDA has received numerous Medical Device Reports (MDRs) for spinal cord stimulators, highlighting potential complications and risks associated with these devices. Between 2016 and 2020, the FDA received 107,728 MDRs, including 428 reports of patient deaths. Common complaints include device malfunction, inadequate pain relief, and potential nerve damage 1. Device Malfunction: Device malfunctions, including charging problems and malfunctions, have been reported. Some patients have reported ele
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The FDA has received numerous Medical Device Reports (MDRs) for spinal cord stimulators, highlighting potential complications and risks associated with these devices. Between 2016 and 2020, the FDA received 107,728 MDRs, including 428 reports of patient deaths. Common complaints include device malfunction, inadequate pain relief, and potential nerve damage 1. Device Malfunction: Device malfunctions, including charging problems and malfunctions, have been reported. Some patients have reported ele
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