Robuta

https://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/infusion-pump-recall-infusion-pump-thermal-damage-issue-smiths-medical Infusion Pump Recall: Infusion Pump Thermal Damage Issue from Smiths Medical | FDA Infusion Pump Thermal Damage Issue from Smiths Medical infusion pumpsmiths medicalrecallthermaldamage https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/smiths-medical-asd-inc-617147-10012021 Smiths Medical ASD Inc. - 617147 - 10/01/2021 | FDA Medical Device Reporting/Misbranded smiths medicalasdincfda https://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/ventilator-recall-smiths-medical-removes-parapac-plus-ventilators-due-loosened-or-detached-patient Ventilator Recall: Smiths Medical Removes ParaPAC Plus Ventilators due to Loosened or Detached... paraPAC Plus P300 and P310 are emergency and transport portable ventilators. The patient outlet connector may be loose or detached, impacting ventilation.