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A
C
C
LYX
OMPONENT
OLLECTION
C
1 – I
HAPTER
NTRODUCTION
1-16
S
O
'
M
YSTEM
PERATOR
S
WARNING: Remove and discard the kit if any fluid leaks
are observed after it is primed. If you detect a leak in the kit
at any time, stop the procedure, do not reinfuse, and discard
the blood product.
WARNING: Opening the clamp between the sampling
container "Y" and the anticoagulant line "Y" after the
system self-checks and before venipuncture may cause
non-sterile air to enter the kit. If this occurs, discard this kit
and restart the procedure with a new kit.
WARNING: Failure to spike the saline solution prior to
initiating the prime sequence may cause non-sterile air to
enter the kit. If this occurs, discard the kit and restart the
procedure with a new kit.
WARNING: Base the volume of the product(s) to be
collected on the maximum allowable target collection
volume(s) and on sound medical judgment, conforming to
applicable regulations and guidelines set by the appropriate
health regulating agencies.
WARNING: Do not attempt to reinfuse blood components
following fluid leaks or spills, when the instrument is
operating with unexpected noise or vibration, or when a
procedure is ended due to persistent redness in the plasma
tubing line coming from the centrifuge. In these instances,
the products must be discarded.
WARNING: If an alarm or interruption occurs while the
system is processing the red cell product after procedure
completion, a small amount of blood components may enter
the red cell preservation solution container. Dispose of all
potentially biohazardous materials per standard operating
procedures.
WARNING: Do not proceed with manual reinfusion of red
cell container contents if there are air bubbles in the donor
line. Any air in the line may be infused into the donor and
might cause an air embolism.
WARNING: The operator should constantly monitor any
manual reinfusion. The air detector does not function
during manual fluid return.
WARNING: Do not attach a donor to the instrument while
it is in test mode. Test mode includes safety checks to
ensure blood is not being processed.
ANUAL
07-19-01-518 – January 2009
Functionally Closed Kit
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