CLASS I Food recall · Reported 14 Nov 2012 · FDA Enforcement Report
Starbucks Protein Bistro recalled by Flying Food Group
Flying Food Group is recalling Starbucks Protein Bistro, distributed in 19 states. The recall was initiated on 6 Oct 2012 and the FDA has classified it as Class I.
Check your package
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-0632-2013
- FDA event ID
- 63440
- Recalling firm
- Flying Food Group, Newark, NJ
- Brand
- Starbucks
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 6 Oct 2012
- FDA classified
- 6 Nov 2012
- Reported
- 14 Nov 2012
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Other Reasons
- Product category
- Dips & Spreads
Timeline
| 6 Oct 2012 | Recall initiated by company | |
| 6 Nov 2012 | Classified by FDA | +31 days |
| 14 Nov 2012 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Starbucks Protein Bistro Boxes contain Honey Peanut Butter Squeeze Packs which are involved in Justin's Nut Butter expanded recall.
Product as listed by the FDA
Starbucks Protein Bistro Box, Net Wt 6.8 OZ (193g), Contains Cage-free egg, white Cheddar Cheese, multigrain muesli bread with honey peanut butter spread and fruit.
Where it was distributed
CT, MA, NY, NJ, PA, DE, MD, DC, VA, GA, FL, IL, WI, MN, IN, TX, AZ, NV, and CA
ArizonaCaliforniaConnecticutDistrict of ColumbiaDelawareFloridaGeorgiaIllinoisIndianaMassachusettsMarylandMinnesotaNew JerseyNevadaNew YorkPennsylvaniaTexasVirginiaWisconsin
Stores named: Starbucks
Questions about this recall
Why was it recalled?
Starbucks Protein Bistro Boxes contain Honey Peanut Butter Squeeze Packs which are involved in Justin's Nut Butter expanded recall.
Which lots are affected?
Enjoy by Dates: 8/10/212-10/06/12 Best By Dates of Peanut Butter: 7/14/13; 7/26/13; 7/27/13; 7/28/13; 7/29/13; 8/9/13; 8/10/13; 8/13/13; 8/14/13; 8/15/13; 8/26/13; 8/27/13; 8/28/13; 8/29/13; 8/30/13
Where was it sold?
CT, MA, NY, NJ, PA, DE, MD, DC, VA, GA, FL, IL, WI, MN, IN, TX, AZ, NV, and CA
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 I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
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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