The Food and Drug Administration (FDA) informs the public that FDA Advisory No. 2019-257, “Voluntary Recall of Lactum Infant Powder 0-6 Months (350 grams) with Batch No. PL9GDL5B” dated 05 September 2019 is hereby lifted.
After due evaluation of the submitted documents of the Market Authorization Holder (MAH), the FDA has determined that the requirements for the termination of the voluntary recall has been satisfactorily met to properly destroy the affected batch in accordance with FDA Circular No. 2016-012, known as the Guidelines on Product Recall.
The issuance of this advisory shall not in any manner preclude this Office from issuing subsequent orders it may deem necessary and appropriate, should there be findings of any violation of the company to the existing laws, rules, and regulations.
Dissemination of this advisory to all concerned is hereby requested.