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Recall of the DLP® Femoral Arterial Cannula product and DLP® Femoral Cannula and Insertion Kits, Medtronic

2015.06.16

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03724/15

For further information as well as details concerning the device please see the enclosed Advisory Notice of the manufacturer.

Recall of the DLP® Femoral Arterial Cannula product and DLP® Femoral Cannula and Insertion Kits, Medtronic , Download_VeroeffentlichtAm_EN PDF, 33KB, File does not meet accessibility standards