MMB of Louisiana Pasteurized Donor Human Milk, Volume: 3 oz, Cal/Oz: 19, 0.9 g/dL Protein, packaged in a clear plastic b
Summary
The FDA issued a Class III for MMB of Louisiana Pasteurized Donor Human Milk, Volume: 3 oz, Cal/Oz: 19, 0.9 g/d by Mothers' Milk Bank of Louisiana at Ochsner Baptist. Reason: Potential physical contamination: dark spot was noticed on the bottom of container..
Details
Source
Food Recall
External ID
H-0938-2026
Action Date
2026-06-17
Status
Terminated
Category
food
Product Description
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
Lot/Code Info: Batch: 002307-1, 002307-2 EXP: 08/24/2026
Quantity Affected: 32 bottles
Reason for Recall
Potential physical contamination: dark spot was noticed on the bottom of container.
Distribution
LA
Type: Voluntary: Firm initiated
Recall Initiated: 2026-06-03
Company
New Orleans, LA
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 191 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Mothers' Milk Bank of Louisiana at Ochsner Baptist) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Mothers' Milk Bank of Louisiana at Ochsner Baptist have FDA actions?
This is the only FDA action we have on record for Mothers' Milk Bank of Louisiana at Ochsner Baptist in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0938-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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