Check the Batch
Class ITerminated in FDA datasetRecall initiated Oct 2, 2012

Starbuck Protein Bistro Box, 6.80 oz. package

Recalling firm: Gretchen's Shoebox Express

Why it was recalled

The 0.5 oz. single-serve Honey Peanut Butter squeeze packs in the Starbuck Protein Bistro Boxes containing peanut that has a potential to be contaminated with Salmonella.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Nov 21, 2012.

Check your package

Compare the exact product and package details with the label you have.

ProductStarbuck Protein Bistro Box, 6.80 oz. package, UPC 762111881502. The Starbuck Protein Bistro Box contains the 0.5 oz. single-serve Honey Peanut Butter Blend squeeze pack with the UPC 894455000391.
Package size6.80 oz
UPC762111881502, 894455000391

FDA code information

Enjoy By dates: 09/02/12 to 09/27/12, 9/28/12, 9/30/12-10/6/12. The 0.5 oz. single-serve Honey Peanut Butter squeeze pack has the Best By dates: 7/14/13, 8/10/13, 8/13/13, 8/14/13, 8/15/13, and/or 8/26/13.

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Starbuck Protein Bistro Box, 6.80 oz. package, UPC 762111881502. The Starbuck Protein Bistro Box contains the 0.5 oz. single-serve Honey Peanut Butter Blend squeeze pack with the UPC 894455000391.

Extracted codes and context

TypeCode / valueContext
UPC762111881502Starbuck Protein Bistro Box, 6.80 oz. package, UPC 762111881502. The Starbuck Protein Bistro Box contains the 0.5 oz. single-serve Honey Peanut Butter Blend squeeze pack with the
UPC894455000391ns the 0.5 oz. single-serve Honey Peanut Butter Blend squeeze pack with the UPC 894455000391.

Original FDA recall reason

The 0.5 oz. single-serve Honey Peanut Butter squeeze packs in the Starbuck Protein Bistro Boxes containing peanut that has a potential to be contaminated with Salmonella.

Recall details

Recall number
F-0139-2013
Event ID
63340
FDA status
Terminated
Initiated
Oct 2, 2012
Reported
Oct 24, 2012
Classified
Oct 17, 2012
Terminated
Nov 21, 2012
Quantity
approximately 16, 752 units
Location
Seattle, WA, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

Product was distributed at cafe stores in Oregon and Washington only. There are no Canadian consignees.

FDA source record · F-0139-2013

Data updated September 16, 2026. View official FDA data ↗

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