Food Recall Check
Class I · High risk Terminated Initiated Oct 5, 2012 (14 years ago)

Starbucks brand Protein Bistro Box recall

Recalled by Honolulu Baking Company, Ltd. · Honolulu, HI, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Firm used recalled 0.5 oz., single serve squeeze packs of Honey Peanut Butter in their Starbucks Brand Protein Bistro Packs which have been implicated in the Sunland Inc recall.

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

Starbucks brand Protein Bistro Box. cage free egg, white cheddar cheese, multigrain muesli bread, apple slices, red grapes and peanut butter packet. Net weight: 6.8 oz. Starbucks Bistro box UPC 762111881502; Justin's honey Peanut Butter blend UPC 894455000391. Honolulu Baking Co. Honolulu, HI 96813

Quantity: 146,311 boxes since 9/1/2010

Food: Cheese Fresh fruit Bread & bakery

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.

Enjoy By Dates of 9-2-10 - 3-28-12 and 9-1-12 - 10-1-12. for Bistro Boxes. Best Buy Dates for peanut packets: 4/11/11 _ 12/7/12; 7/27/13 and 7/29/13.

Where it was sold

Hawaii

FDA's distribution note: HI distribution only on island of Oahu.

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. 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
Honolulu Baking Company, Ltd.
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 5, 2012
In FDA report of
Nov 14, 2012
Terminated
Nov 7, 2012
FDA recall number
F-0633-2013 · event 63519
Official record
FDA enforcement report search

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