FDA Recall United States Terminated 2026 recordClass III
Mothers' Milk Bank of Louisiana at Ochsner Baptist
- Product
- MMB of Louisiana Pasteurized Donor Human Milk, Volume: 3 oz,…
- Published
- June 17, 2026
- Distribution
- LA
Mothers' Milk Bank of Louisiana at Ochsner Baptist Recall: Foreign object found in a bottle.
United States
TerminatedClass II
- Company
- Mothers' Milk Bank of Louisiana at Ochsner Baptist
- Product
- Donor human milk in 3 oz. plastic bottles.
- Recall date
- February 11, 2020
- Terminated
- April 10, 2020
- Source
- FDA
Reason for recall
Foreign object found in a bottle.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Donor human milk in 3 oz. plastic bottles. | Not published in this source record | 60 total bottles | Batch 000525-1 and Batch 000525-2 |
Distribution
- Product was shipped in the state of LA.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0773-2020
- Event ID
- 85032
- Status
- Terminated
- Classification
- Class II
- Company
- Mothers' Milk Bank of Louisiana at Ochsner Baptist
- Product description
- Donor human milk in 3 oz. plastic bottles.
- Quantity
- 60 total bottles
- Reason
- Foreign object found in a bottle.
- Recall initiation date
- February 11, 2020
- Report date
- March 11, 2020
- Classification date
- Not published in this source record
- Termination date
- April 10, 2020
- Distribution pattern
- Product was shipped in the state of LA.
- UPC, lot, and code information
- Batch 000525-1 and Batch 000525-2
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Mothers' Milk Bank of Louisiana at Ochsner Baptist
Other recalls from Mothers' Milk Bank of Louisiana at Ochsner Baptist
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Louisiana | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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