Patient is not experiencing any symptoms or side effects.Patient just got released from the hospital, due to being fluid overloaded.No other information available.Patient had only recalled cassettes.Both lot numbers on patient's hand are defective and recall affected: 4329617, 4298336.Iv remodulin pt.No add'l info, details, or dates available.Pump return tracking info is not available.Photographs were not provided.This is a continuous infusion.Set flow rate and volume delivered are unk.Position of the pump when alarm occurred is unk.Did the reported product fault occur while in use with the pt? yes; did the product issue cause or contribute to pt or clinical injury? unk if that caused; is the actual cassette available for investigation? yes; did we replace the cassette? replacing; did the pt have add'l cassettes they were able to switch to? no; if no, what was the pt instructed to do in able to continue their infusion? sending new cassettes prior to next change; is the infusion life sustaining? yes; what is the outcome of the event? resolved.Reported to (b)(6) by pt/caregiver.
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