Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:19793
Brand Name:Arrow Super Arrow-Flex Percutaneous Sheath Introducer
Model:CL-07635 CL-07735 and CL-07835
Affected:Multiple
Software version:
Recalling Organisation:InterMed Medical Ltd
71 Apollo Drive
Albany
AUCKLAND 1311
Contact Information:0800 333 444
Manufacturer:Arrow International Inc
Issue:Manufacturer has issued a recall for the product due to potential packaging damage. Therefore the sterility of the product cannot be guaranteed. if a non sterile product is used there is potential for infection to occur.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:23/2/2016
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