Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:20513
Brand Name:Merit/47258/Manifold Kits
Model:
Affected:H875600, H895239, H829
Software version:
Recalling Organisation:InterMed Medical Ltd
71 Apollo Drive
Albany
AUCKLAND 1311
Contact Information:0800 333 444
Manufacturer:Merit Medical Systems Inc
Issue:Due to supplier moulding defect in the drip chamber prior to use and during prep, when contrast is drawn out of the contrast bottle air may be drawn into the contrast fluid channel from the vent channel resulting in the contrast having excessive air bubbles which can cause the burette to empty quickly and the blue ball to drop to the bottom of the chamber interfering with the contrast administration.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:24/8/2016
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