Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:22388
Brand Name:ETEST Teicoplanin 256 (TP) SPB and Foam packaging
Model:
Affected:Catalogue number Foam: 412461 & 522018, Pack size 30 and 100
Software version:
Recalling Organisation:Medi'Ray New Zealand Ltd
53-55 Paul Matthews Road
Albany
Auckland 0632
Contact Information:0800 633 472
Manufacturer:Biomerieux SA
Issue:Following an assessment of ETEST Teicoplanin with Staphylococcus spp., we observed an underestimation of MIC values by at least 1 dilution for Coagulase Negative Staphylococci (CoNS); even though the MIC essential agreement at +/- 1 dilution is > 95% between ETEST TP256 and the reference method Agar Dilution (AD) for Staphylococcus spp.
Recall action type:Correction
Recall action:Manufacturer to issue advice regarding use
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:20/12/2017
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