LittleOak Natural Goat Milk Infant Formula
Reason No pre-market notification and Mixing instructions not in ounces
LittleOak Natural Goat Milk Follow On Infant Formula recall
Recalled by The Little Oak Company Ltd · Auckland, N/A, New Zealand
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
No pre-market notification and Mixing instructions not in ounces
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
LittleOak Natural Goat Milk Follow On Infant Formula (Stage 2); packaged in 800g (1.8lbs) tin cans - six cans per case.
Quantity: 15,600
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Batch No. L-M-23-54, MANF16411 and MANF16564 Product No. FPG006 Best By: 26/5/2025, 17/4/2023, 5/7/2025
Where it was sold
Alaska Alabama Arkansas California Colorado Connecticut District of Columbia Florida Georgia Hawaii Iowa Idaho Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Montana North Carolina Nebraska New Hampshire New Jersey New Mexico Nevada New York Ohio Oklahoma Pennsylvania Puerto Rico Rhode Island South Carolina South Dakota Tennessee Texas Utah Virginia Vermont Washington Wisconsin Wyoming
FDA's distribution note: WY, CA, NY, GA, IL, UT, MD, CO, PA, VT, TX, IN, FL, CT, HI, SC, MN, LA, NJ, MI, WA, OH, KY, NM, ID, MO, OK, NV, AR, NE, IA, MA, VA, TN, NC, AK, AV, AL, NH, SD, WI, PR, RI, KS, ME, MT, DC
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- The Little Oak Company Ltd
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 11, 2023
- In FDA report of
- Oct 18, 2023
- Terminated
- Nov 2, 2023
- FDA recall number
- F-0009-2024 · event 93022
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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