Recall notification -SmartSite Syringe Administration Set

Feb 28, 2019

BD is conducting a voluntary medical device recall of SmartSite Syringe Administration Set (lot number referenced in the table above). The recall is being conducted due to leaking of the syringe administration set, which may result in delay or interruption of infusion, under-infusion, contamination of the fluid path and HCP exposure to infusates.

If you require further assistance, please contact Customer Advocacy at 888-812-3266, 24 hours a day/7 days a week.


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