During testing at the user facility, the device did not alarm when a distal occlusion was present.The device was returned to the biomedical department with a note that stated, "keeps saying check syringe." no tracking information was provided; therefore, specific patient information, pump programming, or event details were not available.There were no reports of any adverse patient events and no reported delays of critical therapies while the device was in clinical use.No additional information was provided.
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