Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:21553
Brand Name:Flocare Gastrostomy Tubes
Model:
Affected:Flocare Gastrostomy tube (G-tube) Ch10 - ENFit, Ch14 - ENFit, ) Ch16 - ENFit, Ch18 - ENFit, Ch20 - ENFit
Software version:
Recalling Organisation:Danone Nutricia NZ Limited
56-58 Aintree Avenue
Airport Oaks
Mangere
Auckland 2022
Contact Information:
Manufacturer:Nutricia HealthCare SA
Issue:The manufacturer has received reports that the connector from the Flocare G-tube ENFit in some occasions detaches. This situation generally occurs while disconnecting the ENFit G-tube from the ENFit feeding set or ENFit syringe.
Recall action type:Correction
Recall action:Manufacturer to issue advice regarding use
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:20/6/2017
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