CLASS I Food recall · Reported 17 Jul 2024 · FDA Enforcement Report

Farmalac 0-12 Low lactose powdered infant formula with iron recalled

Dairy Manufacturers is recalling Farmalac 0-12 Low lactose powdered infant formula with iron, distributed in Texas. The recall was initiated on 24 May 2024 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codes24 044 1 FBLE 352-1 02/13/2024 AUG/2025 24 068 1 FBLE 352-1 03/08/2024 SEP/2025
Quantity recalled5376 cans

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1465-2024
FDA event ID
94683
Recalling firm
Dairy Manufacturers, Prosper, TX
Classification
Class I
Status
Terminated
Recall initiated
24 May 2024
FDA classified
5 Jul 2024
Reported
17 Jul 2024
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Other Reasons
Product category
Baby Formula

Timeline

24 May 2024Recall initiated by company
5 Jul 2024Classified by FDA+42 days
17 Jul 2024Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The firm has not submitted the required premarket notification, parents and caregivers should understand that the products have not been evaluated to determine whether they meet U.S. food safety and nutritional standards.

Product as listed by the FDA

Farmalac 0-12 Low lactose powdered infant formula with iron 12.4 oz cans

Where it was distributed

Throughout Texas

Texas

Questions about this recall

Is Farmalac 0-12 Low lactose powdered infant formula with iron recalled?

Yes. Dairy Manufacturers recalled Farmalac 0-12 Low lactose powdered infant formula with iron on 24 May 2024. The recall is Class I and its status is Terminated. Recall number F-1465-2024.

Why was it recalled?

The firm has not submitted the required premarket notification, parents and caregivers should understand that the products have not been evaluated to determine whether they meet U.S. food safety and nutritional standards.

Which lots are affected?

24 044 1 FBLE 352-1 02/13/2024 AUG/2025 24 068 1 FBLE 352-1 03/08/2024 SEP/2025

Where was it sold?

Throughout Texas

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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