Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:21537
Brand Name:Bard Australia Pty Ltd - Catheter balloon inflation system, single-use
Model:
Affected:Product Code CL3030, Lot numbers 15045606, 15075821
Software version:
Recalling Organisation:Pharmacy Retailing (NZ) Ltd t/a Healthcare Logistics
54 Carbine Road
Mt Wellington
AUCKLAND
Contact Information:09 969 0705
Manufacturer:Perouse Medical
Issue:The manufacturer has identified that the Caliber Inflation Device may be at risk of containing a crack in the primary packaging, resulting in a breach of the sterile barrier.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:13/6/2017
Hide menus
Show menus
0 1 2 4 5 6 7 9 [ /