Fresh Recalls

FDAClass III · Food · Recall H-0938-2026 · Recalled June 17, 2026

MMB of Louisiana Pasteurized Donor Human Milk recall — Mothers' Milk Bank of Louisiana at Ochsner Baptist

Agency report date: June 17, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
MMB of Louisiana Pasteurized Donor Human Milk
Company / brand
Mothers' Milk Bank of Louisiana at Ochsner Baptist
Lot / serial / date codes
Batch: 002307-1, 002307-2 EXP: 08/24/2026
Distribution
LA
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class III: not likely to cause adverse health consequences.

Affected product: MMB of Louisiana Pasteurized Donor Human Milk

3. Open the official notice or contact

Official recall ID
H-0938-2026
Brand
Mothers' Milk Bank of Louisiana at Ochsner Baptist
Classification
Class III
Units affected
32 bottles
Recall status
Terminated
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
New Orleans, LA, United States
Firm address
2700 Napoleon Ave, N/A, 70115-6914

Identifying details (verbatim from the notice)

Product codes / lots
Batch: 002307-1, 002307-2 EXP: 08/24/2026
Distribution
LA
Firm notified the public via
Visit
FDA event ID
99155
Recall initiated
June 3, 2026
FDA classified
June 9, 2026
FDA report date
June 17, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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