Related manufacturer report number: 2017865-2023-16372, related manufacturer report number: 2017865-2023-18100, related manufacturer report number: 2017865-2023-18101.It was reported that a patient presented with fever, erythema soreness, and infection.The physician elected to explant the pacemaker system.The patient condition was not known.
|
Related manufacturer report number: 2017865-2023-16372.Related manufacturer report number: 2017865-2023-18100.Related manufacturer report number: 2017865-2023-18101.Additional information received notes that the patient condition was stable before, during, and after the procedure.
|