Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:25217
Brand Name:UniCel DxH Slidemaker
Model:UniCel DxH Slidemaker Stainer (DxH SMS), UniCel DxH Slidemaker Stainer II (DxH SMS II)
Affected:
Software version:
Recalling Organisation:Beckman Coulter NZ Ltd
Suite 2, Level 4
30 St Benedicts Street
Newton
AUCKLAND
Contact Information:0800 446 109
Manufacturer:Beckman Coulter Inc
Issue:The manufacturer has identified that if the Sample Aspiration Module (SAM) is not in a safe position while performing cleaning or troubleshooting procedures, the dispense probe may be inadvertently bent. The DxH SMS/DxH SMS II is designed to generate the error message Stripper Motor movement cannot be verified and inactivates the Slidemaker when a probe is bent, however in rare circumstances a slightly bent probe is not detected. This condition may lead to carryover.
Recall action type:Recall
Recall action:Product to be exchanged
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:15/10/2019
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