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Medspira Recalls

1 recall on record · September 6, 2017 to September 6, 2017 · Medical Devices

September 6, 2017Medical DevicesFDA

Medspira, Llc recalls mcompass 2-channel Balloon Catheters The mcompass Biofeedback Anorectal Manometry System is for use on patients requi

Hazard: Potential failure in the balloon bond in the inner catheter stem, leading to the separation of the balloon from the inner stem, leaving it in the rectal cavity.

Medspira Recalls | RecallWatchUSA