Frozen Pasteurized Human Milk in glass bottles. Label contains lot code followed by expiration date (month day year) and the description of the product which states Mature Milk. There is a Mothers' Milk Bank logo

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    MMBMT-050114-71-1 through MMBMT-050114-71-12. 050114 represents the date the milk was pasteurized; 71 refers to the batch number; 1 refers to the bottle number. A total of 46 bottles were pasteurized for batch 71.
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Mothers' Milk Bank of Montana
Reason for Recall:
Donor answered NO to question #32 "In the last 28 days, have you ever had a vaccine for measles, mumps or rubella?" It was later discovered that she had in fact received live vaccines for influenza, DTAP and MMR after delivery.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Frozen Pasteurized Human Milk in glass bottles. Label contains lot code followed by expiration date (month day year) and the description of the product which states Mature Milk. There is a Mothers' Milk Bank logo

Product Codes/Lot Numbers:

MMBMT-050114-71-1 through MMBMT-050114-71-12. 050114 represents the date the milk was pasteurized; 71 refers to the batch number; 1 refers to the bottle number. A total of 46 bottles were pasteurized for batch 71.

Distribution:

Distributed in: CA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0016-2015

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