Patient checked her inventory last night and all of her cassettes are affected by the smith's recall.She did not have current lot numbers with her and said it was about 6 cassettes affected.She is currently infusing with affected cassette and feeling fine but has said over the last month experienced more headaches an shortness of breath.She is due to mix again tomorrow evening.No further information known.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? no.Is the actual cassette available for investigation? yes.Did we [mfr] replace the cassette? yes.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? na.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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