CLASS II Food recall · Reported 5 Dec 2018 · FDA Enforcement Report

Oreo Limber. 6 dozen recalled by La Casa del Limber

La Casa del Limber is recalling Oreo Limber. 6 dozen per. The recall was initiated on 12 Oct 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesN/A
Quantity recalled34,272 units (distribution dates are from July 9, 2018 - October 11, 2018)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0673-2019
FDA event ID
81428
Recalling firm
La Casa del Limber, Anasco, PR
Classification
Class II
Status
Terminated
Recall initiated
12 Oct 2018
FDA classified
28 Nov 2018
Reported
5 Dec 2018
Type
Voluntary: Firm initiated
Customers notified by
Visit
Product category
Other

Timeline

12 Oct 2018Recall initiated by company
28 Nov 2018Classified by FDA+47 days
5 Dec 2018Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The product label failed to declare wheat as one of its ingredients.

Product as listed by the FDA

Oreo Limber. 6 dozen per case of 6.5 oz each

Where it was distributed

US Domestic Consignees only.

Questions about this recall

Is Oreo Limber. 6 dozen per recalled?

Yes. La Casa del Limber recalled Oreo Limber. 6 dozen per on 12 Oct 2018. The recall is Class II and its status is Terminated. Recall number F-0673-2019.

Why was it recalled?

The product label failed to declare wheat as one of its ingredients.

Which lots are affected?

N/A

Where was it sold?

US Domestic Consignees only.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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