Product description

Flocare Infinity Pack Giving Set MLL W/O DC – Transition
Flocare Infinity Bottle Giving Set – Transition
Flocare Infinity Pack Giving Set W/O DC & W/O MP - Transition
Flocare Infinity Bottle Giving Set W/O MP – Transition
Flocare Infinity Pack Mobile Giving Set – Transition
Flocare Infinity Pack Mobile Giving Set W/O MP - Transition

See a list of details to help identify the product

Reason the product is recalled

There have been reports of ENFit transition adaptors, which are supplied in Australia as a component of Flocare transition giving sets, leaking and/or breaking.

The hazards to consumers

If a transition adaptor is used and it leaks or breaks, it could lead to patients receiving less feed than intended. For some patients, especially critical and/or volume sensitive patients, this can have a negative impact on their health if it not noticed for a significant period of time. Leakage can occur immediately after connection or over time.

What consumers should do

If you or someone you care for uses Flocare transition giving sets for tube feeding, you can continue to use them. These products are not being removed from the market.

Please note that this issue only affects you if you use MLL and mobile giving sets that have a white transition adaptor on the patient-end which connects to a luer feeding tube. It does not apply to situations in which the transition adaptor is unscrewed and discarded during connection.

However, if this issue does affect you, you are advised to carefully check transition adaptors for any minor defects, avoid over-tightening connectors, and monitor for leakage after initial connection and again about two hours after connection. If any problems are identified or suspected, replace the transition giving set with a new one.

If you have any questions or concerns about this issue, speak to your health professional. Alternatively, you can contact Nutricia Australia on 1800 060 051.

Details to help identify the product

Supplier running the recall

Nutricia Australia Pty Ltd

Identifying product features

Codes: 595168, 595172, 595174, 595179, 595181, 595182 All batch numbers are affected.

Identifying numbers

Other identifying numbers

Codes: 595168, 595172, 595174, 595179, 595181, 595182
All batch numbers are affected.

Responsible regulators

Regulators are established or appointed by government. They enforce regulations and rules.

Quote PRA number 2016/15159 when contacting a regulator about this recall.

Recall and remedy questions

Contact the Therapeutic Goods Administration if you have:

  • a question about the remedy being offered to you by the business that is responsible for managing this recall, or
  • concerns about the way the business is managing this recall.