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Recall of one lot of POWERFLEX® PRO PTA Dilatation Catheter, Cordis

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 07688/13

Cordis has determined that some units from one lot of POWERFLEX® PRO PTA Dilatation Catheter may have the potential to exhibit slow/no inflation/deflation. The manufacturer recalls the affected lot from the market.

Recall of one lot of POWERFLEX® PRO PTA Dilatation Catheter, Cordis , Download_VeroeffentlichtAm_EN PDF, 299KB, File does not meet accessibility standards