Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:36709
Brand Name:cervical/endometrial Applicator
Model:Brachytherapy applicator, remote afterloading, Cervical/Endometrial
Affected:
Software version:
Recalling Organisation:Elekta Pty Limited - New Zealand Branch
Suite 302, Geyser Building, 100 Parnell Road
Parnell
AUCKLAND 1052
Contact Information:0273-544-793
Manufacturer:Nucletron BV
Issue:The manufacturer are informing customers of a safety concern regarding the detachment of the tip of the Intrauterine tube (IU tube) with a 4mm diameter. Inadequate application of the epoxy adhesive between the tip and the inner and end surfaces of the fibre tube may contribute to tip detachment.
If the tip detaches during a procedure and is retained in the body there is risk of reduced fertility, inflammation and pain.
Recall action type:Correction
Recall action:Manufacturer to issue advice regarding use
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:1/4/2026
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