Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:27347
Brand Name:Novocastra™ Liquid Mouse Monoclonal Antibody CD19
Model:
Affected:65870, 67492, 66328, 65543, 65317, 64945, 64765, 64224, 64432, 63694, 63909, 62948
Software version:
Recalling Organisation:Leica Microsystems Pty Ltd, New Zealand Branch
3/33 Spartan Road
Takanini
Auckland 2105
Contact Information:021 0841 7323
Manufacturer:Leica Instruments Singapore Pte Ltd
Issue:The manufacturer has recently became aware that the affected Novocastra liquid mouse monoclonal may not perform as specified in the IFU to the shelf life indicated on the product labelling. They have also determined that the concentration of the product is lower than that which is indicated on the labelling.
Recall action type:Correction
Recall action:Manufacturer to issue advice regarding use
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:4/3/2021
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