KCB Pista Khatie KCB Bakery Products Corp recall
Recalled by Kashmir Crown Baking LLC · Linden, NJ, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
The firm's Pista Khatie cookies with use by date 16 May 14 were tested by the Canadian Food Inspection Agency (CFIA) and found to contain 70 ppm of undeclared egg allergen. The label for this product states that it does not contain eggs.
Undeclared allergen: Egg
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
KCB Pista Khatie KCB Bakery Products Corp. 56-28 56th Street, Maspeth, NY 11378 Tel: (718) 786-9463 Fax (718) 361-0171 www.kbcusa.com a) Net Wt. 30 OZ (850 G) b) Net Wt. 13 OZ (369 G) Packaged in a plastic clam shell container with stick-on labels.
Quantity: 24 cases x 12 plastic clam shell boxes; 15 cases x 13 clam shel boxes
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.
Use By Date: 16 May 14; 13 oz. package UPC Code: 12042 00129; 30 oz. package UPC Code: 12042 00296
Where it was sold
California
FDA's distribution note: CA, Canada
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to egg; for anyone else the product is generally not a safety concern. 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
- Kashmir Crown Baking LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 17, 2013
- In FDA report of
- Nov 13, 2013
- Terminated
- Apr 19, 2016
- FDA recall number
- F-0121-2014 · event 66579
- Official record
- FDA enforcement report search