Report ID "113277" refers to multiple distinct records, most notably a 2016 FDA adverse event report involving a third-degree burn from a Philips Respironics sleep monitor. Other records under this number include a Louisiana ethics filing, a peer-reviewed orthopedics article, and an Eaton circuit breaker model. For details on the medical device incident, consult the FDA MedWatch Program .
Report ID "113277" refers to multiple distinct records, most notably a 2016 FDA adverse event report involving a third-degree burn from a Philips Respironics sleep monitor. Other records under this number include a Louisiana ethics filing, a peer-reviewed orthopedics article, and an Eaton circuit breaker model. For details on the medical device incident, consult the FDA MedWatch Program .