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
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
- Brand
- Oreo Limber
- 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
- Reason category
- Undeclared Wheat & Gluten
- Product category
- Other
Timeline
| 12 Oct 2018 | Recall initiated by company | |
| 28 Nov 2018 | Classified by FDA | +47 days |
| 5 Dec 2018 | Published 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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