United States
TerminatedClass II
No pre-market notification and Mixing instructions not in ounces
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| LittleOak Natural Goat Milk Follow On Infant Formula (Stage 2); packaged in 800g (1.8lbs) tin cans - six cans per case. | Not published in this source record | 15,600 | Batch No. L-M-23-54, MANF16411 and MANF16564 Product No. FPG006 Best By: 26/5/2025, 17/4/2023, 5/7/2025 |
This recall shares FDA event ID 93022 with 1 other product entry in Public Health Trace.
FDA Recall United States TerminatedTerminated: November 2, 2023Historical recordClass II
Responsible company: The Little Oak Company Ltd
FDA Recall United States TerminatedTerminated: November 2, 2023Historical recordClass II
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.
| State | Distributed |
|---|---|
| Wyoming | 1 |
| California | 1 |
| New York | 1 |
| Georgia | 1 |
| Illinois | 1 |
| Utah | 1 |
| Maryland | 1 |
| Colorado | 1 |
| Pennsylvania | 1 |
| Vermont | 1 |
| Texas | 1 |
| Indiana | 1 |
| Florida | 1 |
| Connecticut | 1 |
| Hawaii | 1 |
| South Carolina | 1 |
| Minnesota | 1 |
| Louisiana | 1 |
| New Jersey | 1 |
| Michigan | 1 |
| Washington | 1 |
| Ohio | 1 |
| Kentucky | 1 |
| New Mexico | 1 |
| Idaho | 1 |
| Missouri | 1 |
| Oklahoma | 1 |
| Nevada | 1 |
| Arkansas | 1 |
| Nebraska | 1 |
| Iowa | 1 |
| Massachusetts | 1 |
| Virginia | 1 |
| Tennessee | 1 |
| North Carolina | 1 |
| Alaska | 1 |
| Alabama | 1 |
| New Hampshire | 1 |
| South Dakota | 1 |
| Wisconsin | 1 |
| Puerto Rico | 1 |
| Rhode Island | 1 |
| Kansas | 1 |
| Maine | 1 |
| Montana | 1 |
| District of Columbia | 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.
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
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View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
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.
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.
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.
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
Public Health Trace does not provide medical advice. The information below explains how to interpret this record and links to relevant official government sources. Review the linked official source for the current, authoritative information.
This record is preserved as published by FDA, as of November 2, 2023.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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.
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