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Class II: temporary or reversible health riskTerminated

Symrise Wow Beef Dry Marinade Seasoning Recall

Wow Beef Dry Marinade Seasoning, 12

Symrise Inc. · Teterboro, NJ

Risk level
Class II
Reported by FDA
Oct 9, 2019
Recall ID
F-0013-2020
Check your lot numberHow we source this data

Summary

Symrise recalled Wow Beef Dry Marinade Seasoning starting Sep 19, 2019. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0013-2020 on Oct 9, 2019. Reason: Undeclared allergen (milk). Status: Terminated.

Why it was recalled

Undeclared allergen (milk).

Product description

Wow Beef Dry Marinade Seasoning, 12.474 kg paper bags

Lot numbers, UPCs & expiration codes

40100007, Best by date: 06/05/2020

Where it was sold

Distributed to one customer in PA.

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-0013-2020
Classification
Class II
Status
Terminated
Recall initiated
Sep 19, 2019
FDA report date
Oct 9, 2019
Quantity
3,617.46 kgs
Recall type
Voluntary: Firm initiated
Recalling firm
Symrise Inc.

Original FDA data

Every field from FDA enforcement report F-0013-2020, exactly as published.

Show all FDA fields
City
Teterboro
State
NJ
Status
Terminated
Country
United States
Event ID
83856
Address
300 North St
Code information
40100007, Best by date: 06/05/2020
Postal code
07608-1204
Report date
Oct 9, 2019
Product type
Food
Recall number
F-0013-2020
Classification
Class II
Recalling firm
Symrise Inc.
Product quantity
3,617.46 kgs
Termination date
Jul 24, 2020
Reason for recall
Undeclared allergen (milk).
Voluntary / mandated
Voluntary: Firm initiated
Product description
Wow Beef Dry Marinade Seasoning, 12.474 kg paper bags
Distribution pattern
Distributed to one customer in PA.
Recall initiation date
Sep 19, 2019
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Oct 3, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0013-2020, published Oct 9, 2019. View the source record (openFDA) · FDA enforcement reports

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

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