CLASS I Food recall · Reported 17 Nov 2021 · FDA Enforcement Report

Bobo's Almond Butter Protein Bar Multipack, Master Case recalled

Simply Delicious is recalling Bobo's Almond Butter Protein Bar Multipack, Master Case with 6 sleeves, distributed nationwide in the US. The recall was initiated on 26 Oct 2021 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot: 1H18403L; Best By: May 15, 2022
Quantity recalled254 master cases of six 4-pack sleeves = 6,096 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-0169-2022
FDA event ID
88940
Recalling firm
Simply Delicious, Boulder, CO
Brand
Bobo's
Classification
Class I
Status
Terminated
Recall initiated
26 Oct 2021
FDA classified
17 Nov 2021
Reported
17 Nov 2021
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Peanuts
Product category
Granola Bars

Timeline

26 Oct 2021Recall initiated by company
17 Nov 2021Classified by FDA+22 days
17 Nov 2021Published in enforcement report+0 days

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

Reason for recall

Almond Butter Bars contain undeclared peanuts.

Product as listed by the FDA

Bobo's Almond Butter Protein Bar, 2.2 oz., 4-pack Multipack, Master Case with 6 sleeves. UPC 8-29262-00201-6 (Individual bar) UPC 8-29262-00326-6 (4-Pack Multipack) UPC 8-29262-00370-9 (Master Case of 6 sleeves) Storage ambient.

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Almond Butter Bars contain undeclared peanuts.

Which lots are affected?

Lot: 1H18403L; Best By: May 15, 2022

Where was it sold?

Nationwide

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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