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Food recall · FDA · Published December 9, 2016

O'Pelle Enterprises, Inc. recalls Opelle Bakery Egg Bagel (B-105), case of 96 (4 oz.), Frozen Raw.

O'Pelle recalls 96 frozen egg bagels (B-105) with lot codes 369 and below due to missing Yellow 5 label declaration. Consumers should check labels for this specific issue.

🇺🇸 FDA recall #F-1331-2017FoodO'Pelle ›
Take action

Contact the company & request your remedy

Recalling firmO'Pelle Enterprises, Inc.1471 Sw 5th Ct · Pompano Beach, FL 33069-3524
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

O'P: O'Pelle Enterprises recalls 96 frozen egg bagels (B-105) with lot codes 369 and below because the label lacks a required color additive (Yellow 5). This is a labeling issue, not a safety hazard. Read more at govinfonow.com/recall/22646-o-pelle-egg-bagel-recall-missing-yellow-5-label.

Source Summary by GovInfoNow · govinfonow.com/recall/22646-o-pelle-egg-bagel-recall-missing-yellow-5-label · Updated October 8, 2026 · FDA enforcement record: FDA #F-1331-2017

Cite this page

“O'Pelle Egg Bagel Recall: Missing Yellow 5 Label.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22646-o-pelle-egg-bagel-recall-missing-yellow-5-label. Based on FDA recall #F-1331-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1331-2017%22&limit=1).

Why it’s dangerous

The hazard is that the product label does not declare Yellow 5, a color additive. This is a labeling deficiency, not a safety risk. The product itself is safe to eat but must meet labeling requirements.

Who’s affected

Anyone who purchased O'Pelle Egg Bagel (B-105) with lot codes 369 or below. The risk is minimal as this is a labeling issue, not a safety hazard.

How to tell if you have this one

Check for the product name 'Egg Bagel (B-105)', case of 96 (4 oz.), frozen raw, and lot codes 369 and below. The label should show Yellow 5 as a declared ingredient.

  • Brand
    O'Pelle
  • Category
    Food
FDA recall event · 3 products

All 3 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    Distributed only within Florida.
Recall numberProduct, codes & lotsQuantity
F-1330-2017Opelle Bakery Egg Bagel (C-105), case of 60 (3.5 oz.), Frozen Raw.; All lot codes of 86 and below9 cases still within shelf-life at initiation of recall
F-1331-2017Opelle Bakery Egg Bagel (B-105), case of 96 (4 oz.), Frozen Raw.; All lot codes of 369 and below.101 cases still within shelf-life at initiation of recall
F-1332-2017Opelle Bakery Rainbow Bagel (B-110), case of 96 (4 oz.), Frozen Raw.; All lot codes of 26 and below53 cases still within shelf-life at initiation of recall
Based on the official FDA remedy

What to do — step by step

  1. Check Label

    Look for the label declaration of Yellow 5 on the product packaging.

✎ GovInfoNow

Questions people ask

Is this product safe to eat?

Yes, the product is safe to eat. This recall is for labeling compliance, not a safety hazard.

What should I do if I have this product?

Check the label for Yellow 5 declaration. If missing, it is part of the recalled batch with lot codes 369 and below.

How can I tell if I have the recalled product?

The recalled product is O'Pelle Egg Bagel (B-105), case of 96 (4 oz.), frozen raw, with lot codes 369 and below.

Take action

Contact O'Pelle

We’ve drafted a message you can send O'Pelle to request your refund or repair — edit it as you like.

Subject: Recall F-1331-2017 — O'Pelle O'Pelle

Hello,

I own a O'Pelle that is covered by recall F-1331-2017 from O'Pelle.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

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-1331-2017 (December 9, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1331-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA