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Class II: temporary or reversible health riskTerminated

La Casa del Limber Oreo Limber Recall

Oreo Limber

La Casa del Limber, Inc. · Anasco, PR

Risk level
Class II
Reported by FDA
Dec 5, 2018
Recall ID
F-0673-2019
Check your lot numberHow we source this data

Summary

La Casa del Limber recalled Oreo Limber starting Oct 12, 2018. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0673-2019 on Dec 5, 2018. Reason: The product label failed to declare wheat as one of its ingredients. Status: Terminated.

Why it was recalled

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

Product description

Oreo Limber. 6 dozen per case of 6.5 oz each

Lot numbers, UPCs & expiration codes

N/A

Where it was sold

US Domestic Consignees only.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0673-2019
Classification
Class II
Status
Terminated
Recall initiated
Oct 12, 2018
FDA report date
Dec 5, 2018
Quantity
34,272 units (distribution dates are from July 9, 2018 - October 11, 2018)
Recall type
Voluntary: Firm initiated
Recalling firm
La Casa del Limber, Inc.

Original FDA data

Every field from FDA enforcement report F-0673-2019, exactly as published.

Show all FDA fields
City
Anasco
State
PR
Status
Terminated
Country
United States
Event ID
81428
Address
Carr #405, Km. 4.8 Int
Postal code
00610
Report date
Dec 5, 2018
Product type
Food
Recall number
F-0673-2019
Classification
Class II
Recalling firm
La Casa del Limber, Inc.
Product quantity
34,272 units (distribution dates are from July 9, 2018 - October 11, 2018)
Termination date
Jan 10, 2020
Reason for recall
The product label failed to declare wheat as one of its ingredients.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Oreo Limber. 6 dozen per case of 6.5 oz each
Distribution pattern
US Domestic Consignees only.
Recall initiation date
Oct 12, 2018
Initial firm notification
Visit
Center classification date
Nov 28, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0673-2019, published Dec 5, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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