Check the Batch
Class ITerminated in FDA datasetRecall initiated Oct 26, 2021

Bobo's Almond Butter Protein Bar, 2.2 oz., 4-pack Multipack, Master Case with 6 sleeves.

Recalling firm: Simply Delicious, Inc.

Why it was recalled

Almond Butter Bars contain undeclared peanuts.

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: Aug 23, 2022.

Check your package

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

ProductBobo'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.
Package size2.2 oz
UPC829262002016, 829262003266, 829262003709

FDA code information

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

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Full FDA record and distribution details

Original product description

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.

Extracted codes and context

TypeCode / valueContext
UPC829262002016Butter 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 ambie
UPC829262003266ltipack, 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.
UPC829262003709C 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.
best byMay 15, 2022Lot: 1H18403L; Best By: May 15, 2022
lot1H18403LLot: 1H18403L; Best By: May 15, 2022

Original FDA recall reason

Almond Butter Bars contain undeclared peanuts.

Recall details

Recall number
F-0169-2022
Event ID
88940
FDA status
Terminated
Initiated
Oct 26, 2021
Reported
Nov 17, 2021
Classified
Nov 17, 2021
Terminated
Aug 23, 2022
Quantity
254 master cases of six 4-pack sleeves = 6,096 units
Location
Boulder, CO, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Nationwide

FDA source record · F-0169-2022

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

Follow official FDA and manufacturer guidance.