CLASS I Food recall · Reported 23 Aug 2017 · FDA Enforcement Report

Bhufit Bar Chocolate Tart Cherry Pistachio recalled

Laura's Boston Brownies is recalling Bhufit Bar Chocolate Tart Cherry Pistachio. The recall was initiated on 14 Jun 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot code: 13717
Quantity recalled62951 total bars

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-3376-2017
FDA event ID
77705
Recalling firm
Laura's Boston Brownies, San Diego, CA
Brand
Bhufit
Classification
Class I
Status
Terminated
Recall initiated
14 Jun 2017
FDA classified
15 Aug 2017
Reported
23 Aug 2017
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Listeria
Product category
Chocolate

Timeline

14 Jun 2017Recall initiated by company
15 Aug 2017Classified by FDA+62 days
23 Aug 2017Published 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

Potential Listeria monocytogenes contamination.

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

Bhufit Bar Chocolate Tart Cherry Pistachio; Vegan Organic Pea Protein Net Wt. 1.6 oz. (45G)

Where it was distributed

US only - to direct accounts and online customers and sample

Questions about this recall

Why was it recalled?

Potential Listeria monocytogenes contamination.

Which lots are affected?

Lot code: 13717

Where was it sold?

US only - to direct accounts and online customers and sample

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.

Other products in this recall event

8 other products · FDA event 77705

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