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FDA recall, , Moderate risk

University of California Health Donor Human Milk

Pasteurized donor human milk may contain plastic particles.

Recall ended Jul 10, 2026. Still check yours.

What happened

University of California Health Milk Bank in San Diego, California, recalled 60 liters (441 bottles) of donor human milk because the product is potentially contaminated with foreign material (plastic particles). The recall began on May 22, 2026, and was added to the FDA's Enforcement Report on June 2, 2026.

The recalled products are 001165: Standard Pasteurized Donor Human Milk in 100 mL bottles and 001198: Pediatric Pasteurized Donor Human Milk in 200 mL bottles. The product is distributed to medical facilities and directly to consumers through medical facilities, all located in California.

What to do

We don't have product-specific instructions for this recall. FDA's general advice for food recalls:

  1. Return it to the store where you bought it, or throw it away.
  2. Don't give it to anyone else, such as a food bank, or to a pet.

Is your bottle affected?

Affected if its lot code is listed.

  1. 001165: Standard Pasteurized Donor Human Milk; 100 mL bottles 001198: Pediatric Pasteurized Donor Human Milk; 200 mL bottles

    Lot code
    • 001165-1
    • 001165-2
    • 001165-3
    • 001165-4
    • 001165-5
    • 001165-6
    • 001165-7
    • 001165-8
    • 001198
    • 001198-2
    • 00198-3
    • 001198-4
    • 001198-5

Recall details

Company began the recall
Sold in

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

Company
University of California Health Milk BankSan Diego, California
Risk

Moderate risk

Eating it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.

FDA Class II recall · How risk is rated

Event ID
99070
Recall number
H-0948-2026
Quantity recalled
60 liters (441 bottles) total

Timeline

FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.

  1. Company began the recall

  2. Added to FDA's Enforcement Report

  3. Listed on Recall Canary

  4. In FDA's weekly enforcement report

  5. Classified by FDA

  6. Recall ended

  7. Archived

  8. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 12, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)