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Recall FlexCath® steerable sheath, Cryocath
2008.04.07
Product group Injections / Infusions / Transfusions / Dialysis
Reference 01192/08
Cryocath Technologies Inc. recalls all lots of one reference number of the FlexCath® steerable sheath from the market. The flushing side port may contain excessive plastic material which may lead to an impaired function due to a decrease of the inner diameter and to embolism due to loose particles.
Recall FlexCath® steerable sheath, Cryocath , Download_VeroeffentlichtAm_EN