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Minnesota Milk Bank for Babies Recall: Foreign material. (undetermined)

United States

TerminatedClass II

Company
Minnesota Milk Bank for Babies
Product
MN Milk Bank for Babies Pasteurize Donor Human Milk. Volume…
Recall date
December 3, 2024
Terminated
January 21, 2025
Source
FDA

Reason for recall

Foreign material. (undetermined)

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
MN Milk Bank for Babies Pasteurize Donor Human Milk. Volume: 4 fl. oz. / 120 ml. Milk Type: 20 kcal/oz. 1.0 g/dL Total Protein. MN Milk Bank for Babies, Roseville, MN 55113 Not published in this source record 136 bottles Batch 002237-1 Exp Date: 01/01/2025

Distribution

  • MN

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0366-2025
Event ID
95915
Status
Terminated
Classification
Class II
Company
Minnesota Milk Bank for Babies
Product description
MN Milk Bank for Babies Pasteurize Donor Human Milk. Volume: 4 fl. oz. / 120 ml. Milk Type: 20 kcal/oz. 1.0 g/dL Total Protein. MN Milk Bank for Babies, Roseville, MN 55113
Quantity
136 bottles
Reason
Foreign material. (undetermined)
Recall initiation date
December 3, 2024
Report date
January 8, 2025
Classification date
Not published in this source record
Termination date
January 21, 2025
Distribution pattern
MN
UPC, lot, and code information
Batch 002237-1 Exp Date: 01/01/2025
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Telephone
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Minnesota Milk Bank for Babies

Other recalls from Minnesota Milk Bank for Babies

FDA Recall United States Terminated Historical recordClass III

Minnesota Milk Bank for Babies

Product
MN Milk Bank for Babies Pasteurized Donor Human Milk. Volu…
Published
March 24, 2021
Distribution
MN

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Minnesota 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

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