Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:27380
Brand Name:Biopsy Instruments and Kits
Model:
Affected:Lots - 0001356886, 0001369045, 0001364079, 0001369267, 0001369270, 0001364090, 0001364084, 0001369278
Software version:
Recalling Organisation:Pharmacy Retailing (NZ) Ltd t/a Healthcare Logistics
54 Carbine Road
Mt Wellington
AUCKLAND
Contact Information:09 969 0705
Manufacturer:Bard Peripheral Vascular Inc
Issue:An increased trend was identified whereby it was reported that the Penetration Depth Switch (Depth Adjustment Knob) completely detaches from the device during use. The purpose of the Depth Adjustment Knob is to be able to select the desired penetration depth of 18mm or 25mm
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:5/3/2021
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