CLASS II Food recall · Reported 11 Mar 2020 · FDA Enforcement Report

Donor human milk recalled by Mothers' Milk Bank of

Mothers' Milk Bank of Louisiana at Ochsner Baptist is recalling Donor human milk, distributed in Louisiana. The recall was initiated on 11 Feb 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBatch 000525-1 and Batch 000525-2
Quantity recalled60 total bottles

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-0773-2020
FDA event ID
85032
Brand
Donor
Classification
Class II
Status
Terminated
Recall initiated
11 Feb 2020
FDA classified
3 Mar 2020
Reported
11 Mar 2020
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Foreign Material
Product category
Milk

Timeline

11 Feb 2020Recall initiated by company
3 Mar 2020Classified by FDA+21 days
11 Mar 2020Published in enforcement report+8 days

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

Reason for recall

Foreign object found in a bottle.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Donor human milk in 3 oz. plastic bottles.

Where it was distributed

Product was shipped in the state of LA.

Louisiana

Questions about this recall

Why was it recalled?

Foreign object found in a bottle.

Which lots are affected?

Batch 000525-1 and Batch 000525-2

Where was it sold?

Product was shipped in the state of LA.

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 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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