CLASS II Food recall · Reported 19 Jul 2017 · FDA Enforcement Report

Starbucks PB & J Fruit and Veggies recalled by Taylor Farms Texas

Taylor Farms Texas is recalling Starbucks PB & J Fruit and Veggies, distributed in Texas. The recall was initiated on 28 Jun 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesManufacturing Date: 6/25/17 Enjoy By: 6/28/17
Quantity recalled961 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-2535-2017
FDA event ID
77666
Recalling firm
Taylor Farms Texas, Dallas, TX
Classification
Class II
Status
Terminated
Recall initiated
28 Jun 2017
FDA classified
13 Jul 2017
Reported
19 Jul 2017
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Soy
Product category
Other

Timeline

28 Jun 2017Recall initiated by company
13 Jul 2017Classified by FDA+15 days
19 Jul 2017Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Firm was notified by customer of a labeling issue - soy lecithin was not listed as an ingredient of the chocolate covered raisin in a protein box.

Product as listed by the FDA

Starbucks PB & J Fruit and Veggies 7.4 oz. (210 g) UPC: 7 62111 23607 4

Where it was distributed

U.S. distribution to the following; TX only.

Texas

Stores named: Starbucks

Questions about this recall

Why was it recalled?

Firm was notified by customer of a labeling issue - soy lecithin was not listed as an ingredient of the chocolate covered raisin in a protein box.

Which lots are affected?

Manufacturing Date: 6/25/17 Enjoy By: 6/28/17

Where was it sold?

U.S. distribution to the following; TX only.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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