Cyberonics

9 recalls • • Categories: Other Medical Devices, Infusion Pumps, Implants & Prosthetics

Certain Model 3000 programming events can result in miscalculation of parameters stored in the Models 103, 104, 105, and 106 generators. During these programming events, the miscalculations can lead to: " Delivery of more stimulation than intended, resulting in painful stimulation or other common side effects (Model 106 only); " No stimulation in the case of device disablement (Burst Watchdog Timeout), resulting in no therapy to the patient (Model 106 only); " Delivery of less stimulation than intended, resulting in therapeutic settings not being achieved within device specification (Models 103, 104, 105, or 106); and/or " Delays or absence of the 75% and 50% battery life indicators displayed by the programming software (Models 103, 104, 105, or 106).

Nov 13, 2017 Other Medical Devices Nationwide View Details →

Two Model 3000 Programmers were distributed in error by prior to FDA approval of version 1.0.2.2 software.

Dec 2, 2017 Infusion Pumps View Details →

Manufacturing process used to assemble the circuit board may result in some devices experiencing a faster than expected reduction in device longevity.

Jun 13, 2017 Infusion Pumps Nationwide View Details →

Manufacturing process used to assemble the circuit board may result in some devices experiencing a faster than expected reduction in device longevity.

Jun 13, 2017 Infusion Pumps Nationwide View Details →