FDA recall record

University of California Health Milk Bank 001165: Standard Pasteurized Donor Human Milk recall — FDA H-0948-2026

Product is potentially contaminated with foreign material (plastic particles).

Class IIclassification
H-0948-2026official record ID
Jun 10, 2026report date

Recall record at a glance

Official recordH-0948-2026
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmUniversity of California Health Milk Bank
Report dateJun 10, 2026
Recall initiation dateMay 22, 2026
Quantity60 liters (441 bottles) total
LocationSan Diego, CA, United States

Official product description

001165: Standard Pasteurized Donor Human Milk; 100 mL bottles 001198: Pediatric Pasteurized Donor Human Milk; 200 mL bottles No UPC

Why the product was recalled

Product is potentially contaminated with foreign material (plastic particles).

Distribution information

Product is distributed to medical facilities and direct to consumer through medical facility. All facilities and consumers are located in CA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.