Every recall we track for Spes Medica — 5 in all — plus the complaints and injury reports the public filed about them.
Spes Medica recalls Dragonfly Laryngeal Surface Electrodes with specific model numbers due to possible issues with ethylene oxide sterilization processes.
Spes Medica recalls SNS Disposable Urethral Catheter Electrodes due to possible sterilization process deviations. This may affect safety during medical procedures.
Spes Medica recalls Tripolar Hooked Stimulation Probes (L=20mm, Reference SI3H0020S2526D) due to possible ethylene oxide sterilization deviations. This affects intraoperative neurological monitoring devices.
Spes Medica recalls Dragonfly Laryngeal Surface Electrodes with specific model numbers due to potential sterilization process deviations. Affected units may not meet safety standards for surgical use.
Spes Medica recalls 10 Fr urethral catheter electrodes due to possible sterilization process deviations. Affected units have reference number UE006 and lot UR20F2702I. No remedy specified in official notice.
