Labrada Lean Pro 8 Chocolate Tubs Recall: Undeclared Egg Hazard
Labrada Nutrition recalls two chocolate tub sizes due to undeclared egg in product. Consumers should check lot numbers and UPCs listed to determine if affected.
Lower-risk recall
Undeclared egg
Contact the company
What happened, in plain English
Labrada Nutrition is recalling two sizes of Lean Pro 8 Chocolate tubs because they contain undeclared egg. This means the product may not be suitable for people with egg allergies, as the egg is not listed on the label. Read more at govinfonow.com/recall/19188-labrada-lean-pro-8-chocolate-tubs-recall-undeclared-egg-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/19188-labrada-lean-pro-8-chocolate-tubs-recall-undeclared-egg-hazard · Updated October 7, 2026 · FDA enforcement record: FDA #F-1392-2018
Cite this page
“Labrada Lean Pro 8 Chocolate Tubs Recall: Undeclared Egg Hazard.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19188-labrada-lean-pro-8-chocolate-tubs-recall-undeclared-egg-hazard. Based on FDA recall #F-1392-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1392-2018%22&limit=1).
Why it’s dangerous
The product contains egg without being declared on the label. This poses a risk for individuals with egg allergies who may experience allergic reactions if they consume the product.
Who’s affected
People who have purchased the Lean Pro 8 Chocolate tubs with the listed lot numbers or UPCs are affected. Those with egg allergies are at higher risk due to the undeclared egg.
How to tell if you have this one
Check the lot numbers: 083747, 083757, 083767, 083777, 038748, 038758, 017598. Also look for the UPC codes 710779112841 or 710779113411 on the product packaging.
- Brand
Labrada Nutrition- Product
Lean Pro 8 Chocolate 2,268g (5lb) Tub and Lean Pro 8 Chocolate 1,000g (2.2lb) Tub- Category
Food
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 I- Status
Terminated- Distribution
Distributed nationwide throughout the US and the following countries - Vietnam, Dom Republic, Kuwait, Panama, Saudi, Korea, Germany, Iceland, EU, Bermuda, Australia, Jordan
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-1391-2018 | Lean Pro 8 Vanilla 2,268g (5lb) Tub; Lot# 073437, 073447, 073457, 073467, 073477; UPC # 710779112834 | 3517 units |
| F-1392-2018 | Lean Pro 8 Chocolate 2,268g (5lb) Tub and Lean Pro 8 Chocolate 1,000g (2.2lb) Tub; Lot# 083747, 083757, 083767, 083777, 038748, 038758, 017598; UPC# 710779112841 and UPC# 710779113411 | 2976 units |
| F-1393-2018 | Lean Pro 8 Cookies & Cream 1,000g (2.2lb) Tub; Lot# 083707; UPC# 710779113435 | 132 units |
What to do — step by step
Check Product Lot Numbers
Look for lot numbers 083747, 083757, 083767, 083777, 038748, 038758, or 017598 on the tub packaging.
Verify UPC Codes
Confirm the product has UPC codes 710779112841 or 710779113411 to identify if it's part of the recall.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Distributed nationwide throughout the US and the following countries - Vietnam, Dom Republic, Kuwait, Panama, Saudi, Korea, Germany, Iceland, EU, Bermuda, Australia, Jordan” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 6 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Why is there an undeclared egg in these chocolate tubs?
The recall record states the product contains undeclared egg, but does not explain why it was not declared on the label.
Similar recalls
Latest food recalls
Keep exploring
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-1392-2018 (April 24, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1392-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.