“Simply Delicious Bobo's Almond Butter Bars Recall: Undeclared Peanuts.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/13939-simply-delicious-bobo-s-almond-butter-bars-recall-undeclared-peanuts. Based on FDA recall #F-0169-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0169-2022%22&limit=1).
The FDA announced on Oct. 26, 2021, that Simply Delicious, Inc. is recalling Bobo's Almond Butter Protein Bars due to undeclared peanuts. The agency said the recall covers 6,096 units distributed nationwide.
How to tell if you have it
Brand: Simply Delicious
Product: Bobo's Almond Butter Protein Bar, 2.2 oz., 4-pack Multipack, Master Case with 6 sleeves
UPC (Individual bar): 8-29262-00201-6
UPC (4-Pack Multipack): 8-29262-00326-6
UPC (Master Case of 6 sleeves): 8-29262-00370-9
Lot code: 1H18403L
Best By date: May 15, 2022
Units affected: 6,096
The hazard
The FDA stated that the Bobo's Almond Butter Protein Bars contain undeclared peanuts. The recall is classified as Class I.
Context
GovInfoNow's records show Simply Delicious, Inc. has two other recalls on record since May 5, 2016. On March 22, 2021, the company recalled Bobo's Maple Pecan Oat Bars because they contained peanuts. Other recent recalls of similar products include Bazzini Dark Chocolate Coconut Almond Bites (May 23, 2026), Wilco Peanut Co Raw Shelled Peanuts (May 18, 2026), and Fayus OLA-OLA Pounded Groundnuts (June 19, 2026).
How to tell if you have this one
Check for the UPC 8-29262-00201-6 (individual bar), 8-29262-00326-6 (4-Pack Multipack), or 8-29262-00370-9 (Master Case of 6 sleeves).
Brand
Simply Delicious
Product
Bobo's Almond Butter Protein Bar, 2.2 oz., 4-pack Multipack, Master Case with 6 sleeves. UPC 8-29262-00201-6
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product UPCs
Look for the specific UPC codes listed: 8-29262-00201-6, 8-29262-00326-6, or 8-29262-00370-9.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 10 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0169-2022 (October 26, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0169-2022 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.