Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:36650
Brand Name:AngioDynamic Radiology Range
Model:KMP 4Fr x 65cm Angiographic Catheter
Affected:Lot - A2825132
Software version:
Recalling Organisation:Endotherapeutics NZ Limited
2B Target Court
Wairau Valley
Auckland 0627
Contact Information:
Manufacturer:AngioDynamics Inc (US)
Issue:The manufacturer has identified that this is the possibility of a non-conformance component in of the molded hub of the catheter. This non-conformance may prevent the guidewire from passing through the introducer hub while in use.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:12/3/2026
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