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Class I: serious health riskTerminated

May Flower International 3+2 Soda Crackers Recall

3+2 Soda Crackers (CREAM FLAVOUR)(S) packaged in a 4

May Flower International Inc. · Maspeth, NY

Risk level
Class I
Reported by FDA
Aug 1, 2018
Recall ID
F-1676-2018
Check your lot numberHow we source this data

Summary

May Flower International recalled 3+2 Soda Crackers starting Jun 29, 2018. The FDA classified it as Class I (serious health risk) and published enforcement report F-1676-2018 on Aug 1, 2018. Reason: Product contains undeclared milk. Status: Terminated.

Why it was recalled

Product contains undeclared milk.

Product description

3+2 Soda Crackers (CREAM FLAVOUR)(S) packaged in a 4.4 oz, yellow package, UPC: 6 919892 633101

Lot numbers, UPCs & expiration codes

No codes.

Where it was sold

New York

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-1676-2018
Classification
Class I
Status
Terminated
Recall initiated
Jun 29, 2018
FDA report date
Aug 1, 2018
Quantity
8 cases
Recall type
Voluntary: Firm initiated
Recalling firm
May Flower International Inc.

Original FDA data

Every field from FDA enforcement report F-1676-2018, exactly as published.

Show all FDA fields
City
Maspeth
State
NY
Status
Terminated
Country
United States
Event ID
80432
Address
5845 47th St
Code information
No codes.
Postal code
11378-2106
Report date
Aug 1, 2018
Product type
Food
Recall number
F-1676-2018
Classification
Class I
Recalling firm
May Flower International Inc.
Product quantity
8 cases
Termination date
Aug 2, 2018
Reason for recall
Product contains undeclared milk.
Voluntary / mandated
Voluntary: Firm initiated
Product description
3+2 Soda Crackers (CREAM FLAVOUR)(S) packaged in a 4.4 oz, yellow package, UPC: 6 919892 633101
Distribution pattern
New York
Recall initiation date
Jun 29, 2018
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Jul 30, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1676-2018, published Aug 1, 2018. View the source record (openFDA) · FDA enforcement reports

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

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