RecallRadar
LowReported June 17, 2026 (2 weeks ago)

MMB of Louisiana Pasteurized Donor Human Milk, Volume: 3 oz

Recalled by Mothers' Milk Bank of Louisiana at Ochsner Baptist

Food recall

Mothers' Milk Bank of Louisiana at Ochsner Baptist

Class III — least serious

Using this product is not likely to cause health problems, but it breaks an FDA rule (for example, a labeling or packaging issue).

Mothers' Milk Bank of Louisiana at Ochsner Baptist has recalled MMB of Louisiana Pasteurized Donor Human Milk, Volume: 3 oz, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on June 17, 2026 and was initiated on June 3, 2026. It is classified as a Class III recall, which means using this product is not likely to cause health problems, but it breaks an FDA rule (for example, a labeling or packaging issue).

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers MMB of Louisiana Pasteurized Donor Human Milk, Volume: 3 oz, with approximately 32 bottles affected. The company behind the recall is Mothers' Milk Bank of Louisiana at Ochsner Baptist, based in New Orleans, LA. The FDA describes the product as: “MMB of Louisiana Pasteurized Donor Human Milk, Volume: 3 oz, Cal/Oz: 19, 0.9 g/dL Protein, packaged in a clear plastic bottle with white plastic cap”

Why was MMB of Louisiana Pasteurized Donor Human Milk, Volume: 3 oz recalled?

According to the FDA, the stated reason for the recall is: “Potential physical contamination: dark spot was noticed on the bottom of container.”

What should you do?

If you think you may have bought MMB of Louisiana Pasteurized Donor Human Milk, Volume: 3 oz, compare it against the product description and identifying codes (Batch: 002307-1, 002307-2 EXP: 08/24/2026) before using it.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Mothers' Milk Bank of Louisiana at Ochsner Baptist or your local health authority.

About this recall

This recall was distributed in LA. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Terminated
Date reported
June 17, 2026
Recall started
June 3, 2026
Distributed in
LA
What was recalled
MMB of Louisiana Pasteurized Donor Human Milk, Volume: 3 oz, Cal/Oz: 19, 0.9 g/dL Protein, packaged in a clear plastic bottle with white plastic cap
Why it was recalled (as stated by the FDA)
Potential physical contamination: dark spot was noticed on the bottom of container.
How to identify the affected product
Batch: 002307-1, 002307-2 EXP: 08/24/2026
Amount recalled
32 bottles

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was MMB of Louisiana Pasteurized Donor Human Milk, Volume: 3 oz recalled?+

According to the FDA: Potential physical contamination: dark spot was noticed on the bottom of container.

How serious is this recall?+

Class III — least serious. Using this product is not likely to cause health problems, but it breaks an FDA rule (for example, a labeling or packaging issue).

What should I do if I have MMB of Louisiana Pasteurized Donor Human Milk, Volume: 3 oz?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-0938-2026. Information last synced from the FDA on July 5, 2026.