Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:25228
Brand Name:TFX Athlone - EZ-IO Infusion Kit, Intraosseous
Model:
Affected:All Lot/Batch Numbers: 9018P-EU-005, 9018P-VC-005 - 9001P-EU-005, 9001P-VC-005 - 9079P-EU-005, 9079P-VC-005
Software version:
Recalling Organisation:Teleflex Medical New Zealand
OFFICE 011, 110 CARLTON GORE ROAD
Newmarket
Auckland 1023
Contact Information:027 476 4009
Manufacturer:Teleflex Medical Europe Ltd
Issue:The manufacturer has recently received complaints reporting that the safety cap attached to needles within the EZ-IO needle sets may become dislodged exposing the needle and potentially causing the needle to protrude through the packaging. If this issue is not detected, the immediate risk of exposure to the affected devices is needle stick injury to the clinician or health care professional.
Recall action type:Correction
Recall action:Manufacturer to issue advice regarding use
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:25/10/2019
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