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.