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Sarap Asian Fusion Recall: Undeclared wheat and soy lecithin

United States

TerminatedClass II

Company
Sarap Asian Fusion
Product
Miso Milo Chocolate (cookies); A Sarap Asian Fusion Product…
Recall date
September 12, 2018
Terminated
December 12, 2018
Source
FDA

Reason for recall

Undeclared wheat and soy lecithin

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Miso Milo Chocolate (cookies); A Sarap Asian Fusion Product; Net Wt. 70 G/Cookie; Contains: Flour, eggs, Baking Soda, Baking Powder, Milk Powder, White Sugar, Brown Sugar, Salt, Butter, Miso, Milo cacao, vanilla extract, milk chocolate. MFG at 12042 West St. Garden Grove, CA 92840 Not published in this source record unknown not yet provided

Distribution

  • Online to customers in AE
  • AK
  • AL
  • AR
  • AZ
  • CA
  • CO
  • CT
  • DE
  • FL
  • GA
  • GU
  • HI
  • IL
  • IN
  • JK
  • KS
  • KY
  • LA
  • MA
  • MD
  • MI
  • MN
  • MO
  • NC
  • ND
  • NE
  • NH
  • NJ
  • NM
  • NV
  • NY
  • OH
  • OK
  • OR
  • PA
  • RI
  • SC
  • TN
  • TX
  • UT
  • VA
  • WA
  • WI
  • WV
  • & WY.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0023-2019
Event ID
81015
Status
Terminated
Classification
Class II
Company
Sarap Asian Fusion
Product description
Miso Milo Chocolate (cookies); A Sarap Asian Fusion Product; Net Wt. 70 G/Cookie; Contains: Flour, eggs, Baking Soda, Baking Powder, Milk Powder, White Sugar, Brown Sugar, Salt, Butter, Miso, Milo cacao, vanilla extract, milk chocolate. MFG at 12042 West St. Garden Grove, CA 92840
Quantity
unknown
Reason
Undeclared wheat and soy lecithin
Recall initiation date
September 12, 2018
Report date
October 17, 2018
Classification date
Not published in this source record
Termination date
December 12, 2018
Distribution pattern
Online to customers in AE, AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IL, IN, JK, KS, KY, LA, MA, MD, MI, MN, MO, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, & WY.
UPC, lot, and code information
not yet provided
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Press Release
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 81015 with 3 other product entries in Public Health Trace.

FDA Recall United States Terminated Historical recordClass II

Sarap Asian Fusion

Product
Ube Cookies & Cream (cookies); A Sarap Asian Fusion Product…
Published
October 17, 2018
Distribution
Online to customers in AE, AK, AL, AR, A…

View recall →

FDA Recall United States Terminated Historical recordClass II

Sarap Asian Fusion

Product
Matcha Chocolate (cookies); A Sarap Asian Fusion Product;…
Published
October 17, 2018
Distribution
Online to customers in AE, AK, AL, AR, A…

View recall →

FDA Recall United States Terminated Historical recordClass II

Sarap Asian Fusion

Product
Black Sesame White Chocolate (cookies); A Sarap Asian Fusio…
Published
October 17, 2018
Distribution
Online to customers in AE, AK, AL, AR, A…

View recall →

Responsible company: Sarap Asian Fusion

Other recalls from Sarap Asian Fusion

FDA Recall United States Terminated Historical recordClass II

Sarap Asian Fusion

Product
Ube Cookies & Cream (cookies); A Sarap Asian Fusion Product…
Published
October 17, 2018
Distribution
Online to customers in AE, AK, AL, AR, A…

View recall →

FDA Recall United States Terminated Historical recordClass II

Sarap Asian Fusion

Product
Matcha Chocolate (cookies); A Sarap Asian Fusion Product;…
Published
October 17, 2018
Distribution
Online to customers in AE, AK, AL, AR, A…

View recall →

FDA Recall United States Terminated Historical recordClass II

Sarap Asian Fusion

Product
Black Sesame White Chocolate (cookies); A Sarap Asian Fusio…
Published
October 17, 2018
Distribution
Online to customers in AE, AK, AL, AR, A…

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Alaska 1
Alabama 1
Arkansas 1
Arizona 1
California 1
Colorado 1
Connecticut 1
Delaware 1
Florida 1
Georgia 1
Guam 1
Hawaii 1
Illinois 1
Indiana 1
Kansas 1
Kentucky 1
Louisiana 1
Massachusetts 1
Maryland 1
Michigan 1
Minnesota 1
Missouri 1
North Carolina 1
North Dakota 1
Nebraska 1
New Hampshire 1
New Jersey 1
New Mexico 1
Nevada 1
New York 1
Ohio 1
Oklahoma 1
Oregon 1
Pennsylvania 1
Rhode Island 1
South Carolina 1
Tennessee 1
Texas 1
Utah 1
Virginia 1
Washington 1
Wisconsin 1
West Virginia 1
Wyoming 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.