Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:21687
Brand Name:Sysmex
Model:
Affected:CellaVision DI-60
Software version:
Recalling Organisation:Roche Diagnostics (NZ) Ltd
15 Rakino Way
Mt Wellington
AUCKLAND 1644
Contact Information:0800 363 622
Manufacturer:Roche Diagnostics GmbH
Issue:It has been reported that a possible mix up of results could occur during 'user modification' of a barcode misread in the following circumstances:
1. DI-60 encountered a problem reading the barcode when processing a slide (Slide 1) and a picture of the barcode for Slide 1 is taken by the DI-60.
2. When this occurs the DI-60 provides Slide 1 with a temporary order ID based on the date and time (ie ERRYYYYMMDDhhmmss) and the image of the barcode picture (taken in step 1) is stored in the database and displayed in the order data dialogue against this ERR ID.
3. Following this, a slide (Slide 2) from the slide maker/stainer (SP-10) which has had a barcode misread occurring on the SP-10 and has been.
Recall action type:Correction
Recall action:Manufacturer to issue advice regarding use
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:14/7/2017
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