Food Recall Check
Class II · Moderate risk Terminated Initiated Oct 24, 2013 (13 years ago)

CTF Brand Tapioca Pearl Pandan recall

Recalled by N A Trading Inc · Los Angeles, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

The recall has been initiated due to missing ingredients not being shown in the ingredient list of the packaging. The missing ingredients are: Artificial Color Yellow No. 5 and Brilliant Blue FD&C No. 1.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

CTF Brand Tapioca Pearl Pandan (Green Color), 14oz Plastic Bags, Packaged at 50 bags per case. Packaged in plastic heat-sealed pouch. Brand name is CTF with an illustration of a deer. Product labeling reads in part:"C.T.F. Brand TAPIOCA PEARL***EXPORTED: COMBINE THAI FOODS CO., LTD.***PRODUCT OF THAILAND NET WT:14OZ(400 G)***"

Quantity: 90 cases

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

UPC Code 8 851381 561145. No Lot Codes or Best By Dates. The product only has a UPC code for the public's identification purposes.

Where it was sold

California Georgia Hawaii Kansas Minnesota Missouri New York Ohio Oregon Texas Utah Washington

FDA's distribution note: US states: KS, MN, HI, OH, CA, GA, NY, MO, OR, UT, TX, and Washington D.C.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
N A Trading Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 24, 2013
In FDA report of
Nov 27, 2013
Terminated
Oct 15, 2014
FDA recall number
F-0222-2014 · event 66629
Official record
FDA enforcement report search