Recall notification -BD Gravity IV Sets

Mar 5, 2019

BD is conducting a voluntary medical device recall of BD Gravity IV Sets Catalogues CM42500E-07 and CS42522E-07 (lot number referenced in the table above). The recall is being conducted due to reports of kinked tubing which can lead to occlusion of the sets and in reduction of the rate of infusion. In cases where the kinks are significant, this can lead to difficulty in achieving the desired therapeutic effect.

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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