Angiodynamic Radiology Range

Recalling firm
Endotherapeutics NZ Limited
Product
AngioDynamic Radiology Range. [Device]. Model: KMP 4Fr x 65cm Angiographic Catheter. Affected: Lot - A2825132
Reason
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.
Classification
Class I
Category
medical device recall
Country
New Zealand
Agency
MEDSAFE
Recall date
2026-03-12
Status
Ongoing
Distribution
New Zealand - Hospital/Pharmacy/Laboratory

Official recall notice from MEDSAFE

Recall details on Nibble Recalls: https://trynibble.app/recalls/06887e53-27ec-478e-960a-e9cf193a9848