CLASS III Food recall · Reported 23 Jul 2025 · FDA Enforcement Report
Pasteurized Donor Human Milk plastic recalled
Henry Ford Milk Bank- Jackson is recalling Pasteurized Donor Human Milk plastic, distributed in Michigan. The recall was initiated on 23 Jun 2025 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-0280-2025
- FDA event ID
- 97157
- Recalling firm
- Henry Ford Milk Bank- Jackson, Jackson, MI
- Brand
- Pasteurized Donor
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 23 Jun 2025
- FDA classified
- 17 Jul 2025
- Reported
- 23 Jul 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Particulate Matter
- Product category
- Milk
Timeline
| 23 Jun 2025 | Recall initiated by company | |
| 17 Jul 2025 | Classified by FDA | +24 days |
| 23 Jul 2025 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Foreign material (plastic particulate from outer closure) between immediate closure (foil seal) and outer closure (plastic cap)
Product as listed by the FDA
Pasteurized Donor Human Milk , 4oz plastic bottle
Where it was distributed
MI
Questions about this recall
Why was it recalled?
Foreign material (plastic particulate from outer closure) between immediate closure (foil seal) and outer closure (plastic cap)
Which lots are affected?
Batch 000230-1, Expiration date 1/5/2026 Batch 000235-1 Expiration date 9/5/2025
Where was it sold?
MI
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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|---|---|---|---|---|---|
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