CLASS III Food recall · Reported 1 Oct 2025 · FDA Enforcement Report
Mmbal pasteurized donor human milk (Pdhm) recalled
Mothers' Milk Bank of Alabama is recalling Mmbal pasteurized donor human milk (Pdhm), distributed in Alabama. The recall was initiated on 18 Aug 2024 and the FDA has classified it as Class III.
Check your package
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
- H-0634-2025
- FDA event ID
- 97560
- Recalling firm
- Mothers' Milk Bank of Alabama, Birmingham, AL
- Brand
- Mmbal
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 18 Aug 2024
- FDA classified
- 23 Sep 2025
- Reported
- 1 Oct 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Foreign Material
- Product category
- Milk
Timeline
| 18 Aug 2024 | Recall initiated by company | |
| 23 Sep 2025 | Classified by FDA | +401 days |
| 1 Oct 2025 | Published 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
Potential physical contaminant
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
MMBAL pasteurized donor human milk (PDHM), 100 mL (3.38 fl. oz.), packaged in a BPA-free plastic bottle
Where it was distributed
AL
Questions about this recall
Why was it recalled?
Potential physical contaminant
Which lots are affected?
Batch number: 001868-3 Pool number: 001868 Expiration date: Jan/31/2025
Where was it sold?
AL
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 III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
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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