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Class II: temporary or reversible health riskTerminated

Lenni's Crab Mix Lenny's Maryland Crab Mix Recall

Lenny's Maryland Crab Mix

Lenni's Crab Mix, Inc · Destin, FL

Risk level
Class II
Reported by FDA
Sep 19, 2018
Recall ID
F-1964-2018
Check your lot numberHow we source this data

Summary

Lenni's Crab Mix recalled Lenny's Maryland Crab Mix starting Jul 10, 2018. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1964-2018 on Sep 19, 2018. Reason: Undeclared wheat on the product label. Status: Terminated.

Why it was recalled

Undeclared wheat on the product label

Product description

Lenny's Maryland Crab Mix

Lot numbers, UPCs & expiration codes

TBD

Where it was sold

US Consignees only. (3) 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-1964-2018
Classification
Class II
Status
Terminated
Recall initiated
Jul 10, 2018
FDA report date
Sep 19, 2018
Quantity
408 cases (128oz) 1 gallon
Recall type
Voluntary: Firm initiated
Recalling firm
Lenni's Crab Mix, Inc

Original FDA data

Every field from FDA enforcement report F-1964-2018, exactly as published.

Show all FDA fields
City
Destin
State
FL
Status
Terminated
Country
United States
Event ID
80622
Address
277 Azalea Dr Ste B
Code information
TBD
Postal code
32541-2397
Report date
Sep 19, 2018
Product type
Food
Recall number
F-1964-2018
Classification
Class II
Recalling firm
Lenni's Crab Mix, Inc
Product quantity
408 cases (128oz) 1 gallon
Termination date
Oct 9, 2019
Reason for recall
Undeclared wheat on the product label
Voluntary / mandated
Voluntary: Firm initiated
Product description
Lenny's Maryland Crab Mix
Distribution pattern
US Consignees only. (3) consignees only.
Recall initiation date
Jul 10, 2018
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Sep 13, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1964-2018, published Sep 19, 2018. View the source record (openFDA) · FDA enforcement reports

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

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