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MOTHERS MILK BANK OF NORTH TEXAS Recall: Foreign object found in bottle

United States

TerminatedClass III

Company
MOTHERS MILK BANK OF NORTH TEXAS
Product
Mother's Milk Bank of North Texas 817-810-0071 Pasteurized D…
Recall date
November 30, 2021
Terminated
February 9, 2022
Source
FDA

Reason for recall

Foreign object found in bottle

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Mother's Milk Bank of North Texas 817-810-0071 Pasteurized Donor Human milk Volume: 100mL 1.00 g/dL Protein packaged in sterile BPA free plastic bottle Not published in this source record 54 bottle Batch number: 025958-1 Order number: ORD032148

Distribution

  • TX

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0319-2022
Event ID
89137
Status
Terminated
Classification
Class III
Company
MOTHERS MILK BANK OF NORTH TEXAS
Product description
Mother's Milk Bank of North Texas 817-810-0071 Pasteurized Donor Human milk Volume: 100mL 1.00 g/dL Protein packaged in sterile BPA free plastic bottle
Quantity
54 bottle
Reason
Foreign object found in bottle
Recall initiation date
November 30, 2021
Report date
December 22, 2021
Classification date
Not published in this source record
Termination date
February 9, 2022
Distribution pattern
TX
UPC, lot, and code information
Batch number: 025958-1 Order number: ORD032148
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Other
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: MOTHERS MILK BANK OF NORTH TEXAS

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
Texas 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 III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

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.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.