RecallRadar
ModerateReported December 24, 2025

Pasteurized Donor Human Milk in 4 ounce/120 ml clear plastic bottle…

Recalled by The New York Milk Bank, Inc.

Food recall

The New York Milk Bank, Inc.

Class II — moderate

Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

The New York Milk Bank, Inc. has recalled Pasteurized Donor Human Milk in 4 ounce/120 ml clear plastic bottle…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on December 24, 2025 and was initiated on November 11, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

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 Pasteurized Donor Human Milk in 4 ounce/120 ml clear plastic bottle…, with approximately 66 bottles affected. The company behind the recall is The New York Milk Bank, Inc., based in Valhalla, NY. The FDA describes the product as: “Pasteurized Donor Human Milk in 4 ounce/120 ml clear plastic bottles. The bottles have a foil seal and are capped with a green lid. Bottle size: 120ml”

Why was Pasteurized Donor Human Milk in 4 ounce/120 ml clear plastic bottle… recalled?

According to the FDA, the stated reason for the recall is: “Foreign object.”

What should you do?

If you think you may have bought Pasteurized Donor Human Milk in 4 ounce/120 ml clear plastic bottle…, compare it against the product description and identifying codes (Batch number: 14559-01, Product type: Term milk, Expiration Date: 5/12/26) 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 The New York Milk Bank, Inc. or your local health authority.

About this recall

This recall was distributed in NY. 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
December 24, 2025
Recall started
November 11, 2025
Distributed in
NY
What was recalled
Pasteurized Donor Human Milk in 4 ounce/120 ml clear plastic bottles. The bottles have a foil seal and are capped with a green lid. Bottle size: 120ml
Why it was recalled (as stated by the FDA)
Foreign object
How to identify the affected product
Batch number: 14559-01, Product type: Term milk, Expiration Date: 5/12/26
Amount recalled
66 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 Pasteurized Donor Human Milk in 4 ounce/120 ml clear plastic bottle… recalled?+

According to the FDA: Foreign object

How serious is this recall?+

Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

What should I do if I have Pasteurized Donor Human Milk in 4 ounce/120 ml clear plastic bottle…?+

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-0308-2026. Information last synced from the FDA on July 5, 2026.