Oreo Limber recall
Recalled by La Casa del Limber, Inc. · Anasco, PR, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
The product label failed to declare wheat as one of its ingredients.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
Oreo Limber. 6 dozen per case of 6.5 oz each
Quantity: 34,272 units (distribution dates are from July 9, 2018 - October 11, 2018)
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.
N/A
Where it was sold
FDA's distribution note: US Domestic Consignees only.
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
- La Casa del Limber, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 12, 2018
- In FDA report of
- Dec 5, 2018
- Terminated
- Jan 10, 2020
- FDA recall number
- F-0673-2019 · event 81428
- Official record
- FDA enforcement report search