For those at hospitals with children units, do send send blood products syringes and/or aliquot bags through the pneumatic tube system? If you do did you do a validation for tubing products in syringes?
Do you return to inventory unused blood products issued in syringes or aliquot bags? If you do what is the acceptance requirement?
Thanks for the feed backs. Our facility risk management reports the fatalities to the state and the blood bank to the FDA, so we had to add to the blood bank policy that risk management would notify the state.
Do you have to report a blood product fatality to your respective state? We are having AABB/CAP inspection, the assessor states that it needs to be reported to the state in addition to FDA, CBER and OCBQ. Anyone reporting to their state?
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