Every recall we track for Welch Allyn Inc Mortara — 16 in all — plus the complaints and injury reports the public filed about them.
Welch Allyn recalls ELI 280 Resting Electrocardiographs with specific model numbers and software versions due to malfunction under certain operator workflows. No remedy stated in official notice.
Welch Allyn recalls ELI 380 electrocardiographs with AM12M acquisition module software version 1.5.1 due to failure to meet IEC 60601-2-27 safety standards. Affected units may not be safe for medical use.
Welch Allyn recalls ELI 280 Electrocardiograph with AM12M Acquisition Module software version 1.5.1 that does not meet IEC 60601-2-27 safety standards. Affected units may pose safety risks.
Welch Allyn recalls AM12M Acquisition Module accessories with software version 1.5.1 that do not meet IEC 60601-2-27 safety standards for medical devices.
Welch Allyn recalls Surveyor S12/S19 bedside patient monitors with AM12M acquisition module software version 1.5.1 that do not meet IEC 60601-2-27 safety standards. Affected units have specific serial numbers and part numbers listed in the recall notice.
Welch Allyn recalls ELI 380 electrocardiographs due to potential wireless disconnection from access points, which may disrupt medical monitoring. Affected units have specific part numbers listed in the recall notice.
Welch Allyn recalls H12+ Holter Recorders patient cables due to potential failure to meet defibrillation standards. Affected units may not safely withstand electrical shocks during medical use.
Welch Allyn recalls S4 Wireless Telemeter cables that may not meet defibrillation safety standards. Affected units could pose electrical risks during medical monitoring.
Welch Allyn recalls ELI PC devices that may not meet defibrillation withstand standards for medical use. Affected models include 11066-XXX-50 and 41000-029-XX.
Welch Allyn recalls Q-Stress and XScribe ECG devices due to potential failure to meet defibrillation standards. Affected models include QS-6XX-XXXXX and XSCRIBE-5XX-XXXXX series.
Welch Allyn recalls Q-Tel RMS cardiac/pulmonary rehab systems due to potential defibrillation failure. Affected units may not meet medical electrical safety standards. Contact Welch Allyn for details.
Welch Allyn recalls T12 wireless ECG devices that may not meet international safety standards for defibrillation, requiring immediate action to prevent risks.
Welch Allyn recalls replaceable lead sets for Wireless Acquisition Modules due to potential failure to meet defibrillation withstand requirements in medical electrical equipment.
Welch Allyn recalls Surveyor S12/S19 bedside monitors with specific patient cables due to potential failure in defibrillation tests. Affected units may not meet medical safety standards.
Welch Allyn recalls ELI 10, ELI 350, and other ECG devices that may not meet safety standards for defibrillation. Consumers should contact Welch Allyn for details.
Welch Allyn recalls X12+ Telemeter patient cables that may not meet defibrillation safety standards. Affected units could pose a risk during medical use. Contact Welch Allyn for details.
